Diko : myalgie

myalgie

Informations lexicales

Langue:français, Morpho:min, Morpho:nospace

Informations sémantiques

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polarité

Variantes

Myalgie

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* Mya (maladie de)

Définitions

1. (Médecine) Douleur musculaire.

2. [noun] Pain in a muscle or group of muscles.

3. Une myalgie est une douleur musculaire. C'est le terme générique englobant toutes les douleurs musculaires du corps charnu du muscle.

Liens externes

bn:00056563n

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dbnary:1-myalgie-nom

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umls:C0231528

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umls:C0494973

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wiki:myalgie

Gloses (termes évoquant les sens possibles)

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technique

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Médecine

Associations d'idées

[F]

1000

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médecine

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douleur

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musculaire

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lésion musculaire

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muscle

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myodynie

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sensibilité musculaire

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hyperesthésie musculaire de contact

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gêne musculaire

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douleur dans un muscle

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endolorissement musculaire

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mal musculaire

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Médecine

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technique

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myosite

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douleurs dans les muscles

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myosalgie

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en:other disorders of muscle

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douleurs musculaires

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Douleur

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myonévralgie

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myalgique

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maladie

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fibromyalgie

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maladie de Lyme

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en:myalgia

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douleur articulaire

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en:muscle pain

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quail myopathy

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crampe

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syndrome de l'homme raide

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algie

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en:decreased lactate clearance from muscle after exercise (reported in 1 patient)

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processus pathologique

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en:myodynia

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myopathie alcoolique

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symptôme

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en:myosalgia

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myopathie médicamenteuse

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crampe et spasme

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autres atteintes musculaires

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muscles

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pathologie

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en:decreased muscle mass, especially distally

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en:decreased cytochrome c oxidase (cox) activity and protein

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en:decreased cytochrome c oxidase staining

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en:decreased glutamate oxidation (about 63% of normal)

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en:decreased mitochondrial complex v activity

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en:decreased glycosylation of alpha-dystroglycan (dag1, 128239)

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en:decreased hand grip strength

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en:decreased mitochondrial complex iii activity seen on muscle biopsy

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en:decreased coenzyme q10 content

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en:decreased muscle action potential after warming affected muscle

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en:decreased collagen vi

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en:decreased activity of multiple mitochondrial respiratory complex enzymes

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en:decreased caveolin-3 expression seen on muscle biopsy

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en:decreased caveolae in muscle tissue

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en:decreased amplitude of miniature endplate potentials (mepp)

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en:decreased activity of respiratory complex ii+iii

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en:decreased activity of mitochondrial complex iii

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en:decreased activity of mitochondrial complexes i and iv seen on skeletal muscle biopsy

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en:decreased activity of cytochrome c oxidase in most cases seen on muscle biopsy

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en:decreased activity of complex i and complex iv

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en:decreased activity and protein levels of respiratory chain complexes i, ii, iii, and iv

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en:decreased activities of mitochondrial complexes i, iii, and iv

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en:decreased activities of mitochondrial-encoded respiratory chain complexes

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en:decreased activities of complexes i, iii, and iv, variable

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en:decreased achilles reflex

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en:decreased muscle density on imaging

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en:difficulty rising from a squatting position

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en:decreased muscle mass (especially of limbs)

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en:degrading mitochondria

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en:disruption of the sarcolemmal membrane seen on muscle biopsy

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en:disruption of sarcomeres with disorganization of the z band

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en:disorganized myofilaments seen on muscle biopsy

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en:disorganization of the myofibrillar pattern

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en:difficulty walking up stairs

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en:difficulty running or inability to run

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en:cytoplasmic inclusion bodies (finding)

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en:difficulty in toe walking

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en:deposits immunoreactive to beta-amyloid protein

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en:dependent edema after excess fat has been present for several years

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en:dense membranous structure surrounding nuclei on electron microscopy

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en:delayed motor development (cvs+)

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en:degenerating nerve terminals

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en:decreased muscle mass in the thighs

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en:degenerate mitochondrial on em

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en:deficiency of mitochondrial respiratory enzymes seen on muscle biopsy

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en:defects in lipoate-containing mitochondrial enzyme complexes

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en:defective mitochondrial oxidative phosphorylation of multiple enzymes

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en:defective glycosylation of alpha-dystroglycan seen on biopsy

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en:decrement of the compound muscle action potential on repetitive stimulation

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en:decremental response on 3-hz repetitive nerve stimulation

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en:decreased thiamine pyrophosphate

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en:decreased shoulder muscle mass

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en:decreased sarcolemmal immunostaining for ptrf

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en:decreased postsynaptic folding at the neuromuscular junction

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en:decreased muscle succinate dehydrogenase

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en:decreased ability to run

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en:calf muscle enlargement

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en:cytochrome c oxidase-negative fibers

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en:attacks last 4 to 24 hours

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en:biopsy shows deposition of complement proteins c5b-9 of the membrane attack complex on muscle fibers or in vacuoles

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en:biopsy shows degenerative changes consistent with myopathy

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en:biopsy of adipose tissue shows reduced adipocyte size

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en:bilateral foot drop

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en:biceps brachii atrophy

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en:a subset of patients have aggravation on cold exposure ('cold paresis')

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en:axial weakness

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en:axial muscle hyperextension, episodic

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en:autophagosome

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en:autophagic vacuoles seen on biopsy (in some patients)

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en:attacks usually decrease or disappear after age 40 years

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en:attacks precipitated by rest after exercise

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en:atrophy of type 1 and type 2 fibers

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en:biopsy shows rimmed vacuoles, central nuclei, and variation in fiber size

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en:atrophy of the small muscles in the hands and feet

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en:atrophy of the intrinsic foot and hand muscles

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en:atrophy of neck muscles may occur later

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en:atrophy of ankle and toe extensor (dorsiflexor) muscles

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en:atrophy, mild (in some cases)

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en:atrophic muscle fiber on biopsy

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en:atrophic fibers

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en:ascending muscle weakness (beginning with feet and legs)

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en:arm/shoulder muscle hypoplasia

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en:areflexia due to muscle weakness

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en:apoptotic nuclei

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en:anterior tibial muscles first involved

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en:biopsy shows myopathy without vacuoles

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en:both type 1 and type 2 fiber predominance has been reported

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en:cytochemical and em muscle studies show large, bizarre mitochondria in striated muscle

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en:cold sensitivity has been reported

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en:cranial muscles spared

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en:cox-negative fibers

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en:cox-deficient fibers

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en:cores with lack of oxidative activity and mitochondrial depletion may also be found and extend along length of fiber

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en:cores have abrupt borders within normal regions of the muscle fiber

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en:cores contain densely packed myofilaments

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en:contractures of distal lower limbs

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en:congophilic staining

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en:congophilic eosinophilic inclusions

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en:congophilic amyloid material

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en:congenital, nonprogressive myopathy

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en:combined oxidative phosphorylation deficiency, complexes i and iv

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en:chronic denervation seen on skeletal muscle biopsy

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en:buffalo hump

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en:central nuclei

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en:centrally nucleated skeletal muscle fibers

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en:centralized nuclei may be seen

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en:centralized myonuclei

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en:cap structures, when present, contain disorganized myofibrils and thickened z bands

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en:calf muscle hypoplasia

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en:distal limb atrophy (upper and lower)

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en:calf hypertrophy (uncommon)

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en:calf hypertrophy (less common)

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en:calf hypertrophy (early in the disease)

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en:calf and thigh cramping muscle pains

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en:by fourth decade, many patients need help with ambulation

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en:distal atrophy of the legs

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en:dystrophic changes

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en:distal limb muscle atrophy (less common)

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en:gait abnormalities (occurs later)

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en:glycogen depletion in skeletal muscle

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en:glycogen accumulation seen on biopsy

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en:gluteus maximus and thigh adductors most affected

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en:global muscle weakness

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en:generalized neonatal hypotonia

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en:generalized muscle weakness also seen in symptomatic carrier females

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en:generalized muscle weakness, proximal and distal

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en:generalized muscle wasting

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en:generalized muscle contractions, episodic

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en:generalized limb muscle atrophy

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en:generalized amyoplasia

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en:fragmentation of the neuromuscular junction with pre- and postsynaptic defects

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en:granular deposits in the sarcomeres

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en:foot extensor muscle weakness (later onset)

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en:focal loss of cross striations on muscle biopsy

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en:firm muscles

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en:filamentous inclusions in muscle fibers

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en:fiber type grouping

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en:fiber size variation

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en:fiber-type variability

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en:fat pad between achilles tendon and medial malleolus

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en:fat pads on the hands and feet

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en:fatty replacement in hip muscles and proximal muscles of the lower limb seen on mri

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en:fatty infiltration seen on muscle biopsy

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en:fatty degeneration of muscle seen on mri

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en:gowers sign (in some patients)

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en:greater soleus involvement than gastrocnemii involvement seen on mri

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en:extensor muscle weakness more severe than flexor muscle weakness

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en:hypoplasia of serratus anterior muscle

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en:inability to stand on tiptoes

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en:impaired mitochondrial respiration

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en:immunoreactivity for z-disk proteins

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en:imaging shows muscle atrophy and fatty replacement

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en:hypotonia (untreated hypothyroidism)

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en:hypotonia (45%)

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en:hypotonia, truncal and appendicular

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en:hypotonia, neonatal and later

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en:hypotonia, generalized (in some patients)

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en:hypothenar muscle atrophy

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en:hypoplastic deltoids

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en:hypoplasia of the hand muscles (29%)

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en:hypoplasia of latissimus dorsi muscle

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en:groups of atrophic fibers seen on muscle biopsy (type i fiber predominance)

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en:hypoplasia of cervical paravertebral muscles

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en:hypoglycosylation of alpha-dystroglycan seen on muscle biopsy

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en:hypertrophy of the extensor digitorum brevis muscles

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en:hypertonicity of the lower limbs

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en:hyaline inclusion

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en:histochemically normal type-ii muscle fibers

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en:hip girdle muscle atrophy

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en:hip abductor weakness and atrophy

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en:head drop due to neck muscle weakness

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en:hang weakness

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en:handgrip myotonia

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en:hamstring and quadriceps muscles mildly affected

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en:fasciculations (less common)

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en:exertional leg pain

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en:distal limb muscle atrophy due to peripheral neuropathy (lower limbs are more affected than upper limbs)

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en:distal muscle weakness (first affects anterior leg muscles, then posterior leg muscles)

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en:easily fatigued (finding)

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en:dystrophic features and atrophic fibers seen on muscle biopsy

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en:dystrophic changes seen on skeletal muscle biopsy

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en:dystrophic changes on biopsy

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en:dystrophic changes may be present

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en:angulated atrophic fibers

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en:dorsal and flexor muscles of the forearm are involved

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en:distal skeletal muscle atrophy (after long disease duration)

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en:distal muscular atrophy due to peripheral neuropathy

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en:distal muscle weakness may occur

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en:distal muscle weakness and atrophy of upper and lower limbs due to peripheral neuropathy

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en:distal muscle weakness and atrophy, upper and lower limbs

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en:distal muscle weakness, predominantly lower limbs

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en:edema, subcutaneous, generalized

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en:distal muscle weakness, occurs initially

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en:distal muscle weakness, lower limbs more severely affected than upper limbs

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en:distal muscle wasting, mild

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en:distal muscle atrophy due to neuropathy

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en:distal muscle atrophy due to denervation

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en:distal muscle atrophy (1 patient)

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en:distal muscle atrophy, predominantly affecting the lower limbs

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en:distal muscle atrophy, affecting the lower limbs

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en:distal lower limb muscle weakness and atrophy

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en:distal lower limb anterior compartment weakness

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en:distal limb muscle weakness occurs later

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en:distal limb muscle weakness (less common)

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en:easy fatigue

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en:edema (hands and feet)

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en:exercise intolerance (less common)

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en:emg shows myotonic discharges in the absence of clinical myotonia

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en:exercise intolerance (also seen in some heterozygotes)

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en:exercise-induced weakness

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en:exercise-induced muscle stiffness

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en:excessive neutral fat and free fatty acids in type-i fibers

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en:evidence of reinnervation seen on emg (1 family)

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en:episodic, nonpruritic, nonurticarial, nonpitting edema

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en:eosinophilic inclusions

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en:enlarged vesicles of sarcoplasmic reticulum origin

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en:enlarged nuclei with central pallor

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en:endomysial fibrosis

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en:emg shows reduction of voluntary recruitment

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en:emg shows neurogenic changes consistent with denervation

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en:emg shows myopathy

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en:edema is present at birth and then slowly decreases

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en:emg shows myopathic or neurogenic changes

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en:emg shows myopathic changes

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en:emg shows increased insertion activity and fibrillation

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en:emg shows fibrillation potentials

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en:emg shows fasciculations

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en:emg may show neurogenic changes

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en:emg may showed myotonic discharges

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en:emg and muscle biopsy shows chronic denervation of the peripheral nerves

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en:electron microscopy shows subsarcolemmal accumulations of abnormally shaped mitochondria

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en:electron microscopy shows abnormal mitochondria with disorganized and vacuolated cristae

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en:electromyography shows myotonic discharges

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en:edema reoccurs with infections

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en:angulated fibers

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en:abnormal jitter seen on emg

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en:amyotrophy of the lower limbs (in some patients)

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en:proximal muscle weakness, limb-girdle distribution

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en:ragged red fibers seen on biopsy

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en:ragged-red muscle fibers

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en:ragged-red fibers on muscle biopsy

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en:quadriceps atrophy (later onset)

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en:quadriceps aplasia

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en:pseudoathletic appearance with prominent muscles before disease onset

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en:proximal weakness

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en:proximal muscle weakness more severe than distal muscle weakness

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en:proximal muscle weakness (occasional)

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en:proximal muscle weakness (85% of patients)

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en:proximal muscle weakness, mild (in some patients)

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en:proximal muscle weakness, mild

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en:proximal muscle atrophy (in some patients)

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en:rectus fascia separation

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en:proximal muscles may be mildly affected

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en:proximal lower limb muscle weakness, later (in some patients)

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en:proximal limb muscle weakness initially

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en:proximal and distal muscle atrophy in lower limbs

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en:protein aggregates immunopositive for actin and desmin

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en:prominent veins, lower limbs

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en:prominent muscular appearance

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en:prominent involvement of the biceps brachii muscles

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en:progressive proximal muscle weakness

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en:progressive interictal weakness is common

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en:progressive distal muscle weakness

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en:progression to wheelchair in fourth decade

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en:recovery between attacks

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en:red-ragged fibers (2p21del)

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en:primarily affects lower limbs

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en:ring fibers

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en:shoulder girdle muscle atrophy

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en:shortening of various muscle-tendon groups in legs

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en:shortening of the fascial structures of the palm and fingers

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en:severe muscle wasting and atrophy, primarily in the legs

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en:severe form shows absence of spontaneous activity at birth

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en:severe disability within 20 years of onset

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en:secondary myopathic features

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en:secondary loss of sarcolemmal caveolin-3

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en:secondary hypertrophy

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en:scapuloperoneal muscular atrophy due to denervation

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en:sarcoplasmic inclusions

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en:sarcomere disappearance seen on muscle biopsy

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en:rimmed vacuoles on biopsy

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en:reduced activity of mitochondrial respiratory chains (1 family)

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en:rigidity (uncommon)

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en:rhabdomyolysis may occur

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en:rhabdomyolysis (in some patients)

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en:rhabdomyolysis, episodic

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en:retroperitoneal fibrosis (rare)

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en:respiratory muscles may be involved (more common in juvenile-onset)

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en:replacement of affected muscle tissue with fatty tissue

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en:relative sparing of the rectus femoris

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en:relatively preserved limb strength

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en:redundancy of basal lamina with accumulated debris

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en:reduced muscle tone but normal power

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en:reduced muscle bulk

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en:primary myopathic changes seen on emg

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en:preserved heel standing

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en:shoulder weakness and atrophy

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en:neurogenic changes

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en:normal or increased facial and neck adipose tissue

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en:normal or increased adipose tissue around the neck

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en:normal or decreased facial and neck adipose tissue

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en:normal muscle fiber (hcs)

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en:normal lamp2 staining (309060)

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en:normal dystrophin immunostaining

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en:normal alpha-glucosidase or acid maltase activity (gaa, 606800)

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en:nonspecific myopathic changes without dystrophic or inflammatory changes seen on muscle biopsy

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en:nonspecific myopathic changes

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en:noninflammatory myopathy with rimmed vacuoles and atrophic fibers seen on muscle biopsy

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en:neuropathic or myopathic changes seen on emg

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en:neurogenic changes seen on emg

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en:neurogenic abnormalities seen on emg

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en:normal phosphorylase kinase activity in muscle

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en:nemaline rod formation

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en:nemaline rods (rare)

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en:nemaline bodies occur in type 1 fibers

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en:nemaline bodies are rarely intranuclear

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en:nemaline bodies (rods) on gomori trichrome staining

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en:necrotic and regenerating fibers

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en:necrotic and atrophic fibers with centralized nuclei

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en:neck flexor weakness

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en:nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic)

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en:myxedematous appearance

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en:myotonia seen on emg

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en:myotonia is present in majority of cases

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en:normal or increased truncal adipose tissue

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en:no dystrophic changes

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en:premature exertional muscle weakness

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en:pelvic girdle muscle atrophy

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en:predominance of oxidative fibers

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en:potassium sensitivity has been reported

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en:positive staining for complement c5b-9 membrane attack complex proteins within vacuoles, but not on muscle fiber membrane

•

en:poor musculature

•

en:poor muscle bulk

•

en:poor head control in infancy

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en:poor exercise tolerance

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en:plaques immunoreactive for desmin and alpha-beta-crystallin

•

en:peroneal muscle weakness and atrophy due to peripheral neuropathy

•

en:peroneal muscle atrophy

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en:percussion-induced rapid rolling muscle contractions (pirc)

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en:pelvic muscle involvement occurs later

•

en:pectoralis major hypoplasia

•

en:no muscle fiber necrosis

•

en:paucity or absence of lymph nodes in the axillae and above the inguinal ligaments seen on scintilymphangiography

•

en:patients may have distal or proximal muscle weakness, or both

•

en:patchy muscle fiber degeneration

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en:partial lipodystrophy (abnormal distribution of subcutaneous adipose tissue)

•

en:paradoxical myotonia (myotonia increases with exercise)

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en:pain or cramping during sustained manual activity

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en:painful swelling in aponeuroses

•

en:other mitochondrial complex enzyme activities may also be decreased

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en:onset of weakness in hands and feet

•

en:numerous vacuole-like areas

•

en:no staining for periodic acid schiff (pas)

•

en:no myofibrillar abnormalities or protein aggregation

•

en:shoulder muscle weakness

•

en:skeletal muscle biopsy shows decreased cytochrome c oxidase activity

•

en:amyotrophy, neurogenic

•

en:weakness, axial and limb muscles, upper limb muscles more affected than lower limbs

•

en:'sloping' shoulders due to muscle atrophy

•

en:non-pitting edema

•

en:z-disk streaming

•

en:z-disks with abnormal homogeneous material

•

en:wrist swelling

•

en:wide variation in fiber size

•

en:weakness of the intrinsic hand muscles (in some patients)

•

en:weakness of the anterior tibial muscle and toe extensors

•

en:weakness of neck extensors (rare)

•

en:weakness of anterior compartment tibial muscles

•

en:weakness of ankle and toe extensor (dorsiflexor) muscles

•

en:weakness may be exacerbated by illness or stress

•

en:wasting, especially temporal, neck, and facial muscles

•

en:abnormal aggregates of desmin and filamin c

•

en:walking may be limited

•

en:virtually no active movement at birth (wws)

•

en:variation of myofiber diameter

•

en:variably decreased alpha-dystroglycan expression (dag, 128239)

•

en:variable fiber size

•

en:variable deficiencies of mitochondrial respiratory chain complexes i, iii, and iv

•

en:variability in fiber size

•

en:vacuoles predominantly in type 2 fibers seen on muscle biopsy

•

en:vacuoles are autophagocytic and contain granular and membranous cellular debris

•

en:vacuoles appear to be exocytosing material at the cell surface

•

en:vacuolar myopathy

•

en:vacuolar degeneration

•

en:abdominal wall muscle weakness (later onset)

•

en:abnormal axons with sprouting and swelling

•

en:upper limb weakness

•

en:absence of laminin alpha-2 chain in muscle

•

en:amyloid deposition in muscle fibers occurs rarely

•

en:aggregates contain granular electron-dense material

•

en:affected muscles show atrophy

•

en:adipose tissue shows many adipocytes with multiple small lipid droplets rather than a normal single lipid droplet

•

en:acute rhabdomyolysis

•

en:acquire ability to walk and jump in childhood, but motor regression occurs later

•

en:accumulation of pas-positive polyglucosan material seen on muscle biopsy

•

en:accumulation of abnormal mitochondria

•

en:absence of subcutaneous fat over entire body except buttocks, hips, and thighs

•

en:absence of some scapular muscles (less common)

•

en:absence of necrosis

•

en:absence of muscle pseudohypertrophy

•

en:absence of gamma-sarcoglycan protein

•

en:abnormal changes in the organization of the sarcolemma and the subsarcolemmal membrane cytoskeleton

•

en:abnormal z bands

•

en:abnormal sarcoplasmic reticulum elements

•

en:abnormal muscle fibers with amorphous, granular, or hyaline deposits

•

en:abnormal mitochondria with loss of cristae

•

en:abnormal mitochondrial proliferation

•

en:abnormal mitochondria

•

en:inclusions show positive immunostaining for sqstm1 and ubiquitin

•

en:abnormal iron deposition in mitochondria

•

en:abnormal glycosylation of alpha-dystroglycan seen on muscle biopsy

•

en:abnormal fat distribution

•

en:abnormal fat accumulation in axillae (in some patients)

•

en:abnormal distribution of subcutaneous fat

•

en:usually a unilateral disorder

•

en:upper limb muscle hypoplasia

•

en:skeletal muscle biopsy shows enlarged mitochondria with abnormal cristae decreased mitochondrial complex i activity

•

en:some patients never achieve ambulation

•

en:swelling of the affected areas

•

en:superior rectus atrophy

•

en:subsarcolemmal mitochondrial aggregates

•

en:subsarcolemmal lipofuscin-positive deposits

•

en:subsarcolemmal hyaline bodies in 25-30% type i fibers only

•

en:subsarcolemmal accumulation of enlarged mitochondria with variably sized rectangular or elongated rhomboidal paracrystalline inclusions

•

en:subsarcolemmal accumulations of abnormally shaped mitochondria seen on electron microscopy

•

en:subcutaneous edema

•

en:streaming of the z-disk seen on electron microscopy

•

en:spheroid bodies are composed of fine filamentous (myofibrillar) material

•

en:sparing of the anterior tibial compartment

•

en:sparing of anterior tibialis muscle

•

en:some patients become wheelchair-dependent

•

en:symmetrical muscle wasting

•

en:soft tissue or tendinous calcinosis may occur

•

en:smooth muscle may also become involved

•

en:small endplate

•

en:small, firm, rubbery, flesh-colored nodules most commonly found on the head, neck, and trunk

•

en:slow motor responses to sudden events (i.e., falling)

•

en:slowly-progressive muscle wasting and weakness with humeroperoneal and scapuloperoneal distribution

•

en:skeletal muscle tissue shows depletion of mitochondrial dna (mtdna)

•

en:skeletal muscle shows dystrophic changes

•

en:skeletal muscle may show less severe mtdna deletion

•

en:skeletal muscle biopsy shows reducing bodies

•

en:skeletal muscle biopsy shows minor variation in fiber size

•

en:skeletal muscle biopsy shows hypertrophy of type 1 and 2 muscle fibers

•

en:swelling of the hands and feet, episodic

•

en:symptoms may be induced by heat

•

en:upper arm and pelvic muscle weakness and atrophy (later onset)

•

en:tubular aggregates in type 2 skeletal muscle fibers

•

en:type i fibers with large, irregularly polygonal congophilic hyaline masses and nemaline rods consistent with nonlysosomal protein degradation

•

en:type ii fiber atrophy seen on muscle biopsy

•

en:type 2 muscle fiber atrophy

•

en:type 2 fiber hypertrophy

•

en:type 1 muscle fiber predominance

•

en:type 1 fiber predominance seen on muscle biopsy

•

en:type 1 fiber atrophy seen on muscle biopsy

•

en:type 1 fibers with inclusions containing myh7 protein aggregates

•

en:type 1 and type 2 muscle fibers with 'minicore' regions of sarcomeric disorganization, lack of oxidative activity, and absent mitochondria

•

en:tubulofilamentous nuclear or cytoplasmic inclusions (15-18 nm)

•

en:tubular aggregates seen on muscle biopsy

•

en:tubular aggregates mainly in type 2 fibers and are subsarcolemmal or intermyofibrillar and stain for nadh-tetrazolium reductase

•

en:tubular aggregates (in some patients)

•

en:tenderness of lower extremities

•

en:triceps weakness

•

en:tremor of the upper limb

•

en:tremors subside over the first 2 to 3 months of life

•

en:transient muscle weakness occur in 75% of patients, particularly in the arms and hands

•

en:transient eosinophilic myositis (seen on muscle biopsy) in the first decade

•

en:toe and foot dorsiflexor weakness

•

en:tibialis anterior muscle affected

•

en:thigh hypertrophy

•

en:thickening of the fascial structures of the palm and fingers

•

en:thickened subcutaneous tissue

•

en:thenar eminence hypoplasia

•

en:tendon tears

•

en:inclusions are tdp43-immunoreactive

•

en:increased variability in muscle fiber diameter

•

en:inclusion body myopathy

•

en:relative muscle weakness, especially in pelvic girdle

•

en:scapular muscle atrophy

•

en:sarcoplasmic accumulation of electron-dense granulofilamentous material

•

en:rimmed vacuoles with basophilic granular material

•

en:rimmed vacuoles

•

en:rhabdomyolysis with exercise (in older patients)

•

en:rhabdomyolysis (in some patients) endocrine : hypogonadotropic hypogonadism (rare)

•

en:rhabdomyolysis, episodic and recurrent

•

en:retain some mechanical adipose tissue (joints, orbits, palms, soles)

•

en:respiratory distress (congenital form)

•

en:replacement of myofibers with connective tissue

•

en:relative sparing of the tibialis anterior

•

en:reduced o-mannosyl glycans on alpha-dystroglycan

•

en:secondary decrease of calpain-3 (capn3, 114240) protein expression in muscle

•

en:reduced muscle mass

•

en:reduced lower limb subcutaneous fat

•

en:reduced ankle dorsiflexion

•

en:rectus medial atrophy

•

en:rectus abdominis muscle separation

•

en:rare necrotic fibers

•

en:ragged red fibers (in some patients)

•

en:ragged-red fibers seen on muscle biopsy

•

en:quadriceps muscle spared

•

en:quadriceps atrophy

•

en:pyruvate oxidation defect

•

en:proximal weakness of the lower limbs with longer disease duration

•

en:scapuloperoneal amyotrophy

•

en:secondary loss of merosin and desmin

•

en:proximal muscle weakness occurs later

•

en:skeletal muscle damage

•

en:some subcutaneous adipose tissue may remain on upper arms

•

en:soft tissue vascular malformations

•

en:soft fleshy palms (50%)

•

en:small rounded fibers

•

en:small or absent axon terminals

•

en:small and incompletely fused muscle fibers seen on biopsy

•

en:small, angulated muscle fibers seen on muscle biopsy

•

en:slowly progressive limb-girdle myopathy

•

en:slim, muscular build (in some patients)

•

en:skeletal muscle weakness

•

en:skeletal muscle tissue shows 14 to 45% depletion of mitochondrial dna (mtdna)

•

en:skeletal muscle shows decreased sarcoglycan proteins

•

en:skeletal muscle biopsy shows misplaced mitochondria

•

en:secondary myopathic changes

•

en:skeletal muscle biopsy shows impaired respiratory oxidation

•

en:skeletal muscle biopsy shows fat droplets in sarcoplasm and mitochondria

•

en:skeletal muscle biopsy shows dystrophic changes

•

en:skeletal muscle biopsy showed mitochondrial complex i deficiency (1 family)

•

en:signs of denervation seen on biopsy

•

en:shoulder weakness

•

en:shoulder muscle hypoplasia

•

en:shoulder girdle muscle weakness and atrophy, progressive

•

en:short and thickened z-discs

•

en:shortening of various muscle-tendon groups in feet

•

en:shortening of flexor profundus muscle-tendon unit

•

en:severe muscle hypotonia at birth

•

en:proximal upper limb amyotrophy

•

en:proximal muscle weakness in upper limbs

•

en:sparing of the brachioradialis muscle (gives appearance of 'oblique amyotrophy')

•

en:nuclear clumps

•

en:percussion-induced muscle mounding (muscle rippling)

•

en:pelvic girdle weakness and atrophy

•

en:pelvic girdle muscle weakness (occurs earlier)

•

en:pectoralis muscles may be less involved, leading to inward shrugging posture

•

en:pectoralis hypoplasia

•

en:patients achieve independent ambulation, but may lose it

•

en:partial lipodystrophy (abnormal distribution of adipose tissue)

•

en:paralysis of the lower limbs (later)

•

en:paracrystalline inclusions

•

en:painful swelling in fasciae

•

en:painful muscle cramps

•

en:onset of lymphedema around puberty

•

en:no staining for oxidative enzymes

•

en:peroneal muscle weakness

•

en:no rods

•

en:no ragged-red fibers

•

en:no muscle weakness

•

en:no lipodystrophy in face and neck

•

en:no facial muscle involvement

•

en:normal or increased abdominal adipose tissue

•

en:normal neonatal period may occur before weakness is apparent

•

en:normal mitochondrial morphology (1 patient)

•

en:nonspecific myopathy

•

en:nonspecific myopathic changes seen on biopsy

•

en:nonspecific muscle fiber atrophy

•

en:neuropathic process seen on muscle biopsy

•

en:percussion myotonias

•

en:phagocytic vacuoles with degraded membranous material

•

en:proximal muscle weakness and atrophy (may occur later)

•

en:prominent involvement of the quadriceps femoris muscles

•

en:proximal muscle weakness (in some patients)

•

en:proximal muscle weakness (120270.0002)

•

en:proximal muscle weakness, mild, of shoulder and hip girdle muscles (in some patients)

•

en:proximal muscle weakness, lower limbs, mild

•

en:proximal muscle weakness, less severe

•

en:proximal muscles more often affected

•

en:proximal lower limb muscle weakness, upper and lower (later onset)

•

en:proximal lower limb amyotrophy

•

en:proximal limb muscle weakness (occurs later)

•

en:proximal and distal muscle atrophy

•

en:protein aggregates resembling myofibrillar myopathy may be present

•

en:prominent musculature

•

en:proliferation of fatty tissue in muscle (in some patients)

•

en:poor muscle build

•

en:progressive proximal muscle involvement

•

en:progressive loss of facial adipose tissue

•

en:progressive ectopic ossification (neck, dorsal trunk, proximal limbs, sternocleidomastoid, masseters)

•

en:progressive distal and proximal symmetric limb weakness

•

en:progression to proximal muscle weakness

•

en:presynaptic defect at the neuromuscular junction

•

en:preservation of visceral, neck, and axillary fat pads

•

en:postexercise cmap amplitude facilitation

•

en:positive staining for slow myosin heavy chain

•

en:positive staining for atpase activity at ph of 4.3

•

en:poor sarcomeric structure (in some patients)

•

en:poor muscle mass

•

en:sparing of small hand and finger muscles

•

en:stiffness (uncommon)

•

en:neurogenic changes later in disease seen on emg

•

en:rheumatism, unspecified; lower leg

•

en:muscular dystrophy-dystroglycanopathy (limb-girdle) type c, 5

•

en:progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 4

•

en:progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3

•

en:rheumatism, unspecified; site unspecified

•

en:rheumatism, unspecified; pelvic region and thigh

•

en:rheumatism, unspecified; multiple sites

•

en:rheumatism, unspecified; hand

•

en:rheumatism, unspecified; ankle and foot

•

en:hyperostosis, sternocostoclavicular

•

en:rheumatism, unspecified; upper arm

•

en:rheumatism, unspecified; shoulder region

•

en:rheumatism, unspecified; other

•

en:rheumatism, unspecified; forearm

•

en:carnitine palmitoyltransferase ii deficiency, late-onset

•

en:tenovitis

•

en:groin discomfort

•

en:shoulder discomfort

•

en:pain in left shoulder

•

en:neck discomfort

•

en:hip discomfort

•

en:back distress

•

en:pain in right shoulder

•

en:z-line streaming see on electron microscopy

•

en:z-disk degeneration

•

en:z-band streaming

•

en:wheelchair dependency in 20% of patients by age 40

•

en:polyglucosan body myopathy 1 with or without immunodeficiency

•

en:primary erythromelalgia

•

en:weakness of the extensor muscles of the hands (initially)

•

en:limb-girdle muscular dystrophy type 2s

•

en:pseudotrichiniasis

•

en:cramp and spasm

•

peste bubonique

•

en:myopathy due to sjögren's disease

•

en:progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6

•

en:glycogen storage disease xiii

•

en:muscle aches:find:24h:musculoskeletal system:ord:reported.hiv-ssc

•

en:myopathy, centronuclear, 4

•

en:lactate dehydrogenase deficiency type a

•

en:myoglobinuria, acute recurrent, autosomal recessive

•

en:myopathy, vacuolar, with casq1 aggregates

•

en:muscular dystrophy, limb-girdle, type 2l (disorder)

•

en:muscular dystrophy, limb-girdle, type 1c

•

en:abnormal muscle tone

•

en:welander distal myopathy

•

en:paramyotonia congenita

•

en:functional motor problems

•

en:increased muscle fatiguability

•

en:muscular dystrophy, congenital, 1c

•

en:pain in limb, hand, foot, fingers and toes

•

en:nontraumatic compartment syndrome

•

en:other soft tissue disorders, not elsewhere classified

•

en:neuralgia and neuritis, unspecified

•

en:other specified soft tissue disorders

•

en:other and unspecified soft tissue disorders, not elsewhere classified

•

en:hypertrophy of fat pad of knee

•

en:weakness of the muscles in the anterior compartment of the lower leg (particularly the tibialis anterior muscle)

•

en:weakness of neck muscles may occur later

•

en:structurally abnormal mitochondria

•

en:thenar amyotrophy (rare)

•

en:tubulofilamentous inclusions

•

en:tubular aggregates seen on biopsy

•

en:tubular aggregates mainly in type 1 fibers

•

en:tubular aggregates in muscle fibers may occur

•

en:trunk muscle atrophy

•

en:triceps aplasia

•

en:tremor at birth, involving most skeletal muscle groups, especially jaw muscles and lower limb muscles

•

en:transient neonatal hypotonia (less common)

•

en:tortuous lymphatic tracts

•

en:thin filament shortening and disorganization (in some patients)

•

en:thick palmar fascia

•

en:thickening of fascia of forearm

•

en:tetanus-like muscle contractions

•

en:type 1 fibers are at least 12% smaller than type 2 fibers

•

en:tendinous and tuberous xanthoma

•

en:symptoms are progressive for a few years, and then become stationary

•

en:symmetrical, proximal limb muscle atrophy (pelvic, scapular, trunk muscles)

•

en:swelling of the hands and feet (in 1 patient)

•

en:swelling of the extremities, episodic

•

en:subsarcolemmal nemaline bodies (rods) on gomori trichrome staining

•

en:subsarcolemmal mitochondrial accumulation

•

en:subsarcolemmal hyaline bodies in type 1 fibers only

•

en:subsarcolemmal accumulation of normal mitochondria (in some patients)

•

en:subsarcolemmal accumulations of abnormally shaped mitochondria seen with electronmicroscopy

•

en:subsarcolemmal accumulations of abnormally shaped mitochondria (on electron microscopy)

•

en:subcutaneous fat markedly reduced

•

en:tubulofilamentous nuclear or cytoplasmic inclusions on biopsy

•

en:type 1 fiber atrophy

•

en:weakness of long finger extensor muscles (occurs later)

•

en:vacuolated muscle fibers show reduplication of the basement membrane

•

en:weakness of ankle plantar flexion

•

en:weakness of all intrinsic hand muscles (later)

•

en:weakness and wasting of the lower limbs

•

en:wasted lower leg muscles

•

en:walking delay

•

en:velopharyngeal muscle weakness

•

en:variation of fiber size and shape

•

en:variably decreased activities of mitochondrial respiratory complexes i, ii, and iv

•

en:variable deficiencies of mitochondrial respiratory chain enzymes

•

en:vacuole membranes show atpase reactivity consistent with origin from the sarcoplasmic reticulum

•

en:vacuoles containing neutral lipids seen on muscle biopsy

•

en:vacuoles are autophagocytic

•

en:vacuolar myopathy may occur

•

en:type 1 fiber predominance

•

en:vacuolar membranes immunostain with sarcolemmal proteins

•

en:uterine muscle may be stiff during pregnancy

•

en:usually no myopathic changes on biopsy

•

en:upper limb muscle weakness may be more severe than lower limb weakness

•

en:upper limb involvement occurs later or not at all

•

en:upper limb involvement and distal muscle involvement may occur later in disease course (often by second decade)

•

en:upper and/or lower limbs may be affected

•

en:type ii fiber predominance

•

en:type 2 muscle fiber predominance

•

en:type 2 fiber predominance

•

en:type 2 fiber atrophy see on biopsy

•

en:type 1 muscle fibers with clearly demarcated central 'core' regions of sarcomeric disorganization, lack of oxidative activity, and absent mitochondria

•

en:neurogenic changes seen on emg and biopsy

•

en:neurogenic atrophy seen on muscle biopsy

•

en:increased adipose fibrosis

•

en:mild variability in muscle fiber size

•

en:mri may show cervical spinal cord atrophy

•

en:motor clumsiness

•

en:mitochondrial vacuolization seen on muscle biopsy

•

en:mitochondrial respiratory chain complex i, ii, and iii defect

•

en:mitochondrial paracrystalline inclusion bodies

•

en:mitochondrial dna depletion (20 to 35% of normal) seen on skeletal muscle biopsy

•

en:mitochondrial dna deletion (1 patient)

•

en:mitochondrial complex iii deficiency, isolated, seen on muscle biopsy

•

en:minimal subcutaneous fat

•

en:minicores or core-like regions may be present

•

en:minicores (in some)

•

en:mild weakness of the small hand muscles

•

en:mild proximal muscle weakness (<10% of patients)

•

en:mri shows fatty replacement

•

en:mild muscle atrophy in forearm muscles

•

en:mild decrease in mitochondrial respiratory chain activity

•

en:mildly reduced respiratory enzyme activities except for complex ii

•

en:mildly decreased cytochrome c oxidase activity

•

en:may have proximal muscle weakness later in the disease

•

en:marked variability of fiber size

•

en:marked predominance of slow-twitch, oxidative (type 1) muscle fibers

•

en:marked loss of subcutaneous fat in the limbs, face, and sometimes chest

•

en:mallory-like bodies

•

en:lymphography shows hypoplasia of lymphatic vessels

•

en:lymphedema of upper and/or lower limbs (in some patients)

•

en:lymphedema of the hands (in some patients)

•

en:mri of the thighs shows fatty atrophy with preservation of the biceps femoris in the lateral compartment

•

en:mri shows increased signal intensity in affected muscles consistent with fatty infiltration

•

en:lymphedema (lower limb)

•

en:muscle atrophy in the limbs

•

en:muscle biopsy shows decreased or absent dysferlin staining

•

en:muscle biopsy shows decreased muscle-specific phosphorylase kinase activity

•

en:muscle biopsy shows decreased glycosylation of alpha-dystroglycan

•

en:muscle biopsy shows cytochrome c oxidase-negative fibers

•

en:muscle biopsy shows chronic and active denervation

•

en:muscle biopsy shows atrophy

•

en:muscle biopsy shows abnormal mitochondria

•

en:muscle biopsy shows 60-80-nm tubular aggregates arranged in hexagonal arrays in type 2 fibers

•

en:muscle biopsy may show mild kinetic abnormalities of the achr

•

en:muscle biopsy may show deficiency of multiple mitochondrial respiratory complexes

•

en:muscle biopsy in acute stage shows increased numbers of abnormal mitochondria

•

en:muscle atrophy restricted to the upper limb

•

en:muscle atrophy affecting the upper back and neck muscles

•

en:mtdna depletion seen on muscle biopsy

•

en:muscle atrophy (type i)

•

en:muscle atrophy (1 patient)

•

en:muscle atrophy, proximal and distal (predominant lower limb involvement)

•

en:muscle atrophy, primarily in the legs

•

en:muscle atrophy, mild

•

en:muscle atrophy, especially quadriceps and forearm muscles

•

en:muscle atrophy, diffuse, severe

•

en:muscle amyotrophy

•

en:muscle aches, intermittent

•

en:muscles have a woody consistency on palpation

•

en:multiple mitochondrial dna deletions

•

en:multiple mitochondrial dna (mtdna) deletions (in most cases)

•

en:lymphedema of lower limbs (in some patients)

•

en:lymphedema, hands (rare)

•

en:muscle biopsy shows deficiency of mitochondrial respiratory enzymes i, iii, iv, and iv

•

en:increased mitochondria with abnormal cristae

•

en:internal nuclei seen on biopsy (in some patients)

•

en:intermyofibrillar and subsarcolemmal granulofilamentous protein aggregates

•

en:interfibrillar and subsarcolemmal vacuoles

•

en:inflammatory cells absent

•

en:independent walking may not be achieved

•

en:increased variation in fiber size seen on muscle biopsy

•

en:increased t-2 signal in muscles of lower extremities on mri (in some patients)

•

en:increased subcutaneous truncal adipose tissue

•

en:increased perisarcolemmal calcium deposition

•

en:increased numbers of type 1 fibers

•

en:increased muscle tone (early in life)

•

en:increased muscle glycogen content

•

en:increased lipid

•

en:isolated necrotic fibers

•

en:increased intramuscular fat

•

en:increased internal nuclei in skeletal muscle fibers

•

en:increased intermyofibrillar and subsarcolemmal glycogen

•

en:increased glycogen in muscle

•

en:increased fibrosis

•

en:increased fat and fibrous tissue

•

en:increased fatty and connective tissue in skeletal muscle

•

en:increased endomysial fibrosis

•

en:increased endo- and perimysial connective tissue

•

en:increased echo intensity in affected muscles

•

en:increased connective tissue (in some patients)

•

en:increased centralized nuclei

•

en:interosseus muscles involved

•

en:knee and hip flexor weakness due to peripheral neuropathy

•

en:low muscle mass

•

en:loss of ability to walk in early childhood

•

en:low maximum workload on exercise testing

•

en:lower limb muscle hypotrophy

•

en:lower limbs more often affected

•

en:lower and upper limbs affected

•

en:loss of subcutaneous fat, particularly affecting the limbs

•

en:loss of subcutaneous adipose tissue primarily in gluteal region and lower limbs

•

en:loss of subcutaneous adipose tissue from upper limbs and trunk

•

en:loss of sarcomeric striations

•

en:loss of lower-limb tendon reflexes

•

en:loss of gluteal adipose tissue

•

en:loss of antigravity strength

•

en:loss of ambulation (in some patients)

•

en:lipodystrophy (in some patients)

•

en:lack of adipose tissue on limbs and femorogluteal regions

•

en:lipoatrophy (lower face, upper limb, buttock)

•

en:lipoatrophic appearance

•

en:lipid droplets seen on muscle biopsy

•

en:lipid accumulation in muscle tissue

•

en:limb weakness, proximal followed by distal

•

en:limb muscle weakness and atrophy, distal, neurogenic

•

en:limb lymphedema (in some patients)

•

en:limb-girdle muscular dystrophy

•

en:limb-girdle muscle weakness, proximal, upper greater than lower

•

en:limb-girdle muscle atrophy

•

en:large lipid droplets

•

en:lack of integrin alpha-7 staining

•

en:muscle biopsy shows decreased secondary clefts

•

en:muscle biopsy shows degeneration of muscle fibers, variation in fiber size, fiber splitting, rimmed vacuoles, and central myonuclei

•

en:neonatal hypotonia muscle biopsy shows pas-positive vacuoles

•

en:muscle weakness and atrophy, distal

•

en:myofibrillar disorganization

•

en:myoclonic spasms

•

en:myalgia with febrile episodes (rare)

•

en:myalgia, episodic

•

en:muscular weakness, improving in infancy (medical research council muscle score of 3 to 4)

•

en:muscular dystrophy (in some patients)

•

en:muscular appearance

•

en:muscle weakness of the face and neck, mild to moderate

•

en:muscle weakness is not a feature

•

en:muscle weakness due to peripheral neuropathy

•

en:muscle weakness and atrophy may be asymmetric

•

en:muscle weakness and atrophy, proximal

•

en:muscle weakness after cooling or on warming affected muscle

•

en:myogenic profile on electromyography

•

en:muscle weakness (in some patients)

•

en:muscle weakness (cvs+)

•

en:muscle weakness, variable

•

en:muscle weakness, symmetric, proximal, lower limbs

•

en:muscle weakness, severe, diffuse

•

en:muscle weakness, severe

•

en:muscle weakness, proximal greater than distal

•

en:muscle weakness, proximal and distal, affecting upper and lower limbs

•

en:muscle weakness, proximal, upper and lower limbs affected

•

en:muscle weakness, proximal, pelvic girdle (in severe cases)

•

en:muscle weakness, proximal, limb-girdle

•

en:muscle weakness, proximal, distal, and axial, severe

•

en:myofibromatosis affecting skin, muscle, bone, and viscera

•

en:myopathic and neurogenic changes seen on emg

•

en:muscle weakness, mild, proximal and distal

•

en:myotonic discharges

•

en:nemaline rods may be observed

•

en:nemaline myopathy (in 1 reported male)

•

en:nemaline bodies are usually subsarcolemmal or sarcoplasmic

•

en:nemaline bodies (rods) on gomori trichrome staining seen on muscle biopsy

•

en:nemaline bodies

•

en:necrotic fibers

•

en:necrotic and regenerating muscle fibers

•

en:necrotic and atrophic fibers with centralized nuclei seen on muscle biopsy

•

en:necrosis and degeneration seen on muscle biopsy

•

en:neck muscle hypoplasia

•

en:neck and proximal limb muscle myopathy

•

en:nearly complete absence of mechanical adipose tissue (joints, orbits, palms, soles)

•

en:myotonia is usually not seen

•

en:myopathic changes on pathology

•

en:myotonia is most pronounced in the extremities

•

en:myotonia (usually occurs during rapid voluntary muscle movements after a period of rest)

•

en:myotonia, potassium-sensitive (may be responsive to acetazolamide)

•

en:myosin storage myopathy (in some patients)

•

en:myopathy in approximately 45% of patients

•

en:myopathy (in some patients)

•

en:myopathy, mild to severe

•

en:myopathic pattern seen on emg

•

en:myopathic findings on biopsy have been occasionally reported

•

en:myopathic episodes triggered by exercise, fasting, infection, cold temperatures

•

en:myopathic changes seen on emg and muscle biopsy

•

en:myopathic changes seen on biopsy

•

en:muscle weakness, predominantly proximal (in some patients)

•

en:muscle weakness, lower limbs, during exercise

•

en:muscle biopsy shows dystrophic changes

•

en:muscle biopsy shows myodegenerative changes with beta-amyloid and phosphorylated tau deposits

•

en:muscle biopsy shows sarcoplasmic or subsarcolemmal vacuoles in muscle fibers

•

en:muscle biopsy shows ragged red fibers

•

en:muscle biopsy shows preserved junctional folds

•

en:muscle biopsy shows pleomorphic hyaline, granular, and amorphous deposits that stain with gomori trichrome

•

en:muscle biopsy shows pas-positive glycogen-containing vacuoles

•

en:muscle biopsy shows nonspecific myopathic changes without dystrophic or inflammatory changes

•

en:muscle biopsy shows neurogenic atrophy

•

en:muscle biopsy shows nemaline rods

•

en:muscle biopsy shows necrotic and regenerating fibers

•

en:muscle biopsy shows myopathic or dystrophic changes

•

en:muscle biopsy shows myofibrillar myopathy

•

en:muscle biopsy shows myofibrillar changes

•

en:muscle biopsy shows mitochondrial paracrystalline inclusions

•

en:muscle biopsy shows small fibers with central nuclei and accumulation of mitochondria in the central part of the fibers

•

en:muscle biopsy shows mild dystrophic changes

•

en:muscle biopsy shows loss of myofibrillar organization

•

en:muscle biopsy shows lipid deposition

•

en:muscle biopsy shows inflammation with t cells

•

en:muscle biopsy shows increased subsarcolemmal vacuolar glycogen accumulation

•

en:muscle biopsy shows hypotrophy of type 1 muscle fibers

•

en:muscle biopsy shows groups of small angulated fibers consistent with denervation

•

en:muscle biopsy shows glycogen storage

•

en:muscle biopsy shows fibrosis and increased connective tissue

•

en:muscle biopsy shows fiber type disproportion

•

en:muscle biopsy shows endplate myopathy (see details under neurologic heading)

•

en:muscle biopsy shows dystrophic features (later in disease course)

•

en:muscle biopsy shows sarcoplasmic rods in myofibers

•

en:muscle biopsy shows small rounded fibers

•

en:muscle weakness, limb-girdle, mild

•

en:muscle hypertrophy may occur

•

en:muscle weakness, episodic

•

en:muscle weakness, distal (in some patients)

•

en:muscle weakness, distal, particularly affecting the hands

•

en:muscle wasting due to chronic denervation

•

en:muscle wasting, severe, primarily in the legs

•

en:muscle strength and bulk is preserved

•

en:muscle stiffness (in older patients)

•

en:muscle paralysis, episodic

•

en:muscle pain and cramps following exercise

•

en:muscle pain after exercise

•

en:muscle mri shows fatty infiltration

•

en:muscle mitochondria normal by histochemical analysis

•

en:muscle hypertrophy (meb)

•

en:muscle biopsy shows type 1 fiber predominance

•

en:muscle hyperirritability

•

en:muscle fiber splitting and fibrosis seen on muscle biopsy

•

en:muscle fiber splitting

•

en:muscle fiber necrosis

•

en:muscle fibers may contain abnormal polysaccharide

•

en:muscle fibers are immunoreactive for desmin and vimentin

•

en:muscle cramps may affect jaw muscles

•

en:muscle cramps at rest

•

en:muscle cramps (also seen in some heterozygotes)

•

en:muscle biopsy with small a-fibers, increased pas-positive material, and ringbinden (disoriented myofibrils)

•

en:muscle biopsy shows type i fiber predominance

•

en:muscle biopsy shows type 2 fiber atrophy

•

en:myotonia improves with continued activity ('warm-up phenomenon')

◀

totaki

repos

•

exercice

•

stress

•

inflammation

•

fibromyalgie

•

fatigue

•

•

douleur

•

raideur

•

douleur chronique

•

traitement

•

syndrome

•

muscle

•

médecine

•

musculaire

•

douloureux

wikipédia

[F]

Crampe

•

MeSH

•

biopsie

•

Anatomie

•

muscle biceps brachial

•

Classification internationale des maladies

•

CIM

•

Muscle

•

EMG

•

anatomie

•

Diseases Database

•

MedlinePlus

•

Medical Subject Headings

•

Maladie de Bornholm

•

Fibromyalgie

•

Myopathie

•

Classification internationale des soins primaires

•

Biopsie

•

Rhumatologie

•

Traumatologie

•

traumatologie

•

Neurologie

•

neurologie

•

CISP

•

Myoglobine

•

Électromyogramme

•

Myorelaxant

•

myoglobine

Thèmes/domaines

médecine

•

lésion musculaire

•

pathologie

•

en:medicine

•

Médecine

•

maladies

•

Maladies

Synonymes et quasi-synonymes

douleur musculaire

•

myosalgie

•

myodynie

•

myalgique

•

myonévralgie

•

Mya (maladie de)

•

en:muscle pain

•

maladie de Mya

•

en:myalgia

•

myasthénie

•

•

mégacôlon congénital

Traduction de myalgie

en:myalgia

•

it:mialgia

•

fi:lihassärky

•

en:muscle pain

•

en:myodynia

•

en:myosalgia

Génériques

[F] [H]

douleur

•

processus

•

•

pathologie du muscle strié

•

pathologie

•

pathologie

(maladie)

•

en:sign or symptom

•

affection

•

maladie

•

signes et symptômes

•

en:signs and symptoms

•

en:muscle

•

maladie

(médecine)

•

processus pathologique

•

Mya

Spécifiques

•

myalgie intercostale

•

myalgie cervicale épidémique

•

myalgie des membres inférieurs

•

myalgie cervicale

•

en:epidemic myalgia

•

en:epidemic pleurodynia

Termes dérivés morphologiquement

algie

•

myalgique

Locutions/termes composés

•

syndrome eosinophilie myalgie

•

syndrome éosinophilie-myalgie

•

éosinophilie-myalgie

•

myalgie cervicale épidémique

•

myalgie intercostale

•

non précisées myalgie et myosite

•

douleur liée à la myalgie

•

myalgie des membres inférieurs

Lieux où peut se trouver/dérouler myalgie

muscle strié squelettique

•

muscle volontaire

•

muscle

•

Muscle squelettique

•

en:tibialis anterior muscle

•

tissu musculaire squelettique

•

muscle squelettique

•

muscle strié

•

muscles striés

•

en:striated muscle

•

muscle jambier antérieur

•

en:skeletal muscle

•

Musculum tibialis anterior

•

muscle tibial antérieur

•

en:anterior tibialis muscle

Causes associées à myalgie

neuralgie

•

en:neuralgia

•

névralgie

•

en:paroxysmal nerve pain

•

douleur névralgique

•

en:nerve pain

•

névralgie paroxystique

•

douleur neuropathique

•

maladie des légionnaires

•

en:legionellosis

•

douleur nerveuse

•

légionellose

•

en:olaparib

•

maladie du légionnaire

•

en:legionnaires' disease

•

olaparib

•

en:legionnaire's disease

•

en:neuropathic pain

•

Douleur neuropathique

•

en:Legionnaires' disease

Conséquences associées à myalgie

douleur

Sentiments/émotions associés à myalgie