Le Diko - en:difficulty walking up stairs

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Le Diko - en:difficulty walking up stairs

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le dictionnaire d'associations lexicales
contributif et libre de JeuxDeMots

en:difficulty walking up stairs

Nom

Informations lexicales

Langue:anglais

Associations d'idées

1000

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

•

en:hypoplastic biceps

•

en:proximal limb muscle weakness initially

•

en:generalized muscular appearance from birth

•

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

•

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

•

en:centrally located nuclei seen on muscle biopsy

•

en:distal amyotrophy

•

en:muscle weakness, severe

•

en:muscle weakness usually does not occur

•

en:attacks may present during or after sleep

•

en:biceps aplasia

•

en:distal muscle atrophy due to neurologic disease

•

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

•

en:fatty replacement

•

en:lipoatrophic appearance

•

en:muscle weakness and atrophy, upper and lower limbs

•

en:aggregates contain granular electron-dense material

•

en:replacement of myofibers with connective tissue

•

en:decreased endplate potential and amplitudes

•

en:increased focal mitochondrial density

•

en:lymphography shows hypoplasia of lymphatic vessels

•

en:normal neonatal period may occur before weakness is apparent

•

en:pain or cramping during sustained manual activity

•

en:replacement of affected muscle tissue with fatty tissue

•

en:muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3

•

en:ability to walk up stairs

•

en:edema, subcutaneous, generalized

•

en:calf and thigh cramping muscle pains

•

en:increased subcutaneous truncal adipose tissue

•

en:muscle biopsy shows decrease or absence of cytochrome c oxidase

•

en:muscle hypertrophy of the lower extremities

•

en:calf hypertrophy (in some patients)

•

en:decreased ant1 protein (103220) in muscle tissue

•

en:hand and foot weakness

•

en:edema (hands and feet)

•

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

•

en:loss of subcutaneous fat, particularly affecting the limbs

•

en:muscle atrophy, primarily in the legs

•

en:muscle atrophy affecting the upper back and neck muscles

•

en:predominance of oxidative fibers

•

en:scapuloperoneal weakness

•

en:glycogen deficiency in muscle fibers

•

en:ragged-red fibers seen on muscle biopsy

•

en:hip abductor weakness and atrophy

•

en:multiple mitochondrial respiratory enzymes deficiencies seen on biopsy

•

en:no staining for oxidative enzymes

•

en:positive staining for atpase activity at ph of 4.3

•

en:relative sparing of the tibialis anterior

•

en:myopathy (in some patients)

•

en:progression to proximal muscle weakness

•

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

•

en:type ii fiber predominance

•

en:signs of denervation seen on biopsy

•

en:proximal muscle weakness occurs later

•

en:abnormal mitochondria in skeletal muscle biopsy

•

en:muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12

•

en:finding related to ability to walk down stairs

•

en:shoulder girdle muscle weakness and atrophy, progressive

•

en:gait disturbance

•

en:nemaline bodies (rods) on gomori trichrome staining

•

en:muscle weakness (type i)

•

en:carpopedal spasm

•

en:amorphous granulofilamentous material associated with z-discs

•

en:cold sensitivity has been reported

•

en:attacks precipitated by rest after exercise

•

en:mitochondrial myopathy

•

en:decreased sarcolemmal immunostaining for ptrf

•

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

•

en:difficulty running or inability to run

•

en:toe and foot dorsiflexor weakness

•

en:painful adipose tissue

•

en:myopathic changes seen on emg and muscle biopsy

•

en:respiratory distress (congenital form)

•

en:muscle biopsy shows inflammation with t cells

•

en:climbing stairs - difficulty:find:pt:^patient:ord:optimal

•

en:loose connective tissue

•

en:increased fiber size variability

•

en:emg shows high-frequency spontaneous discharges

•

en:infantile axial hypotonia

•

en:distal limb muscle atrophy due to peripheral neuropathy

•

en:filamentous inclusions in muscle fibers

•

en:loss of truncal subcutaneous adipose tissue

•

en:muscle biopsy shows variation in fiber size

•

en:proximal muscle weakness, lower limbs, mild

•

en:thickening of fascia of forearm

•

en:asymmetric muscle involvement

•

en:distal lower limb muscle weakness and atrophy

•

en:muscle biopsy shows peripheral accumulation of abnormal mitochondria

•

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

•

en:muscle atrophy, especially quadriceps and forearm muscles

•

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

•

en:muscle biopsy shows mild dystrophic changes

•

en:nemaline myopathy (in 1 reported male)

•

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

•

en:type 1 fiber atrophy

•

en:vacuolar myopathy

•

en:difficulty walking on a narrow line

•

en:has difficulty doing (qualifier value)

•

en:electromyographic decrements in some muscles

•

en:inclusions are dnajb6-immunoreactive

•

en:increased muscle lipid content

•

en:loss of subcutaneous adipose tissue in limbs

•

en:muscle biopsy shows neurogenic atrophy affecting both fibers types

•

en:pelvic girdle weakness and atrophy

•

en:scapular muscle weakness

•

en:waddling gait

•

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

•

en:muscle fiber splitting and fibrosis seen on muscle biopsy

•

en:necrotic fibers

•

en:scapular muscle atrophy

•

en:does not walk on uneven surface

•

en:bilateral foot drop

•

en:muscle biopsy shows atrophic fibers

•

en:normal phosphorylase kinase activity in muscle

•

en:necrotic and regenerating fibers

•

en:muscle weakness in forearm muscles

•

en:abnormal aggregates of desmin and filamin c

•

en:exercise intolerance (less common)

•

en:decreased activity of complex i and complex iv

•

en:attacks precipitated by potassium

•

en:decreased activity of mitochondrial complex i

•

en:cellulitis or infection may occur

•

en:tubulofilamentous inclusions

•

en:dense membranous structure surrounding nuclei on electron microscopy

•

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

•

en:generalized muscle weakness also seen in symptomatic carrier females

•

en:muscle weakness, episodic

•

en:muscle pain after exercise

•

en:nemaline bodies are usually subsarcolemmal or sarcoplasmic

•

en:muscle biopsy shows decreased or absent dysferlin staining

•

en:mitochondrial dna deletion (1 patient)

•

en:involves upper and lower proximal muscles

•

en:hypotonia, fixed

•

en:muscle biopsies show variation in fibrodiameter, internal nuclei, atrophy of type i fibers, focal loss of cross- striations, and cores of myofibrillar disruption with associated absence of mitochondria

•

en:muscle weakness, limb-girdle (lower and upper limbs may be affected)

•

en:muscle pain with exercise (in older patients)

•

en:muscle pain (less common)

•

en:muscle fibers contain internal nuclei

•

en:muscle cramps, painful, recurrent

•

en:muscle biopsy shows neurogenic angulated fibers

•

en:muscle biopsy shows multiple mitochondrial dna (mtdna) deletions

•

en:muscle biopsy shows disruption of the sarcolemmal membrane

•

•

en:mtdna deletions seen on muscle biopsy

•

en:mri shows increased connective tissue and fat

•

en:minicore regions are poorly defined and do not extend through entire fiber length

•

en:mildly reduced respiratory enzyme activities except for complex ii

•

en:lymphedema of lower limbs (in some patients)

•

en:nemaline bodies are rarely intranuclear

•

en:loss of subcutaneous and visceral adipose tissue, mild

•

en:loss of gluteal adipose tissue

•

en:loss of ambulation (in some patients)

•

en:loss of ability to walk in early childhood

•

en:myopathy (rare)

•

en:progressive distal muscle weakness

•

en:neurogenic atrophy seen on muscle biopsy

•

en:secondary myopathic changes

•

en:able to walk on uneven surface

•

en:weakness may be exacerbated by illness or stress

•

en:uterine muscle may be stiff during pregnancy

•

en:umbilical hernia

•

en:type 1 fiber atrophy seen on muscle biopsy

•

en:type 1 fibers with inclusions containing myh7 protein aggregates

•

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

•

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

•

en:skeletal myopathy

•

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

•

en:no muscle weakness

•

en:sarcomere disappearance seen on muscle biopsy

•

•

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

•

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

•

en:progressive proximal muscle weakness

•

en:progressive muscle weakness

•

en:lack of adipose tissue on limbs and femorogluteal regions

•

en:phagocytic vacuoles with degraded membranous material

•

en:paradoxical myotonia (myotonia increases with exercise)

•

en:limb lymphedema (in some patients)

•

en:increased fibrosis

•

en:internal nuclei seen on muscle biopsy

•

en:biopsy shows myopathy without vacuoles

•

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

•

en:decremental response on 3-hz repetitive nerve stimulation

•

en:decreased muscle mass in the thighs

•

en:cytoplasmic inclusion bodies (finding)

•

en:cranial muscles spared

•

en:congenital muscular dystrophy (disorder)

•

en:chronic denervation seen on emg

•

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

•

en:calf hypertrophy (uncommon)

•

en:biopsy muscle normal

•

en:depletion of mitochondrial dna

•

en:axial muscle weakness

•

en:ascites (in some patients)

•

en:amyotrophy, distal, upper and lower limbs

•

en:absence of pectoralis minor muscle

•

en:absence of myotonia in infancy (congenital form)

•

en:absence of merosin in muscle

•

en:absence of caveolin-3 staining

•

en:muscle soft, tissue

•

en:filaminopathy, autosomal dominant

•

en:degenerating fibers

•

en:difficulty running and jumping

•

en:intermyofibrillar and subsarcolemmal accumulation of electron-dense material (in some patients)

•

en:global muscle weakness

•

en:independent walking may not be achieved

•

en:increased variation in fiber size seen on muscle biopsy

•

en:increased variability in muscle fiber diameter

•

en:inclusions form a lobulated structure seen on electron microscopy

•

en:hypoplasia of supraspinatus muscle

•

en:hypoplasia of infraspinatus muscle

•

en:hypoglycosylation of alpha-dystroglycan seen on muscle biopsy

•

en:hand muscle atrophy

•

en:gluteus maximus and thigh adductors most affected

•

en:evidence of lymphatic rerouting

•

en:distal amyotrophy (hands and feet)

•

en:edematous hands and feet (1 patient)

•

en:dystrophic changes on biopsy

•

•

en:distal muscle weakness and atrophy

•

en:distal muscle weakness, predominantly affecting the lower limbs

•

en:distal muscle weakness, mild

•

en:distal muscle atrophy (lower limbs more affected than upper limbs)

•

en:distal lower limb muscle weakness

•

en:distal limb muscle weakness and atrophy

•

en:finding related to ability to start and stop walking spontaneously

•

en:enlarged nuclei with central pallor

•

en:abnormalities in myofibril organization

•

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

•

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

•

en:numerous vacuole-like areas

•

en:normal or increased facial adipose tissue

•

en:non-pitting edema

•

en:neuropathic or myopathic changes seen on emg

•

en:neurogenic changes

•

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

•

en:necrosis and degeneration seen on muscle biopsy

•

en:myopathy, x-linked, with excessive autophagy (disorder)

•

en:myalgia with febrile episodes (rare)

•

en:progressive loss of facial adipose tissue

•

en:muscle weakness is not a feature

•

en:muscle weakness increases with age

•

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

•

en:muscle weakness, limb-girdle, mild

•

en:muscle wasting due to chronic denervation

•

en:muscle spasm

•

en:muscle cramps may affect jaw muscles

•

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

•

en:muscle biopsy shows type 1 fiber predominance

•

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

•

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

•

en:muscle biopsy shows increased subsarcolemmal vacuolar glycogen accumulation

•

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

•

en:abnormal mitochondria with paracrystalline inclusions seen on muscle biopsy

•

en:muscular dystrophy, limb-girdle, type 2g

•

en:finding related to ability to initiate walking

•

•

en:wasted lower leg muscles

•

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

•

en:type 2 fiber atrophy see on biopsy

•

en:tubular aggregates in muscle fibers may occur

•

en:triceps aplasia

•

en:thickened subcutaneous tissue

•

en:proximal muscle atrophy (in some patients)

•

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

•

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

•

en:slim, muscular build (in some patients)

•

en:skeletal muscle biopsy shows misplaced mitochondria

•

en:skeletal muscle biopsy shows impaired respiratory oxidation

•

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

•

en:rhabdomyolysis

•

en:ragged red fibers seen on biopsy

•

en:proximal muscle weakness (occasional)

•

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

•

en:usually no myopathic changes on biopsy

•

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

•

en:distal limb muscular weakness due to peripheral neuropathy

•

en:emg shows myotonic changes

•

en:emg shows myopathic and neurogenic changes

•

en:emg shows chronic denervation

•

en:edema reoccurs with infections

•

en:easy bruisability of lower extremities

•

en:dorsal and flexor muscles of the forearm are involved

•

en:distal muscle weakness may occur

•

en:distal muscle weakness, occurs initially

•

en:distal lower limb anterior compartment weakness

•

en:deposits immunoreactive to beta-amyloid protein

•

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

•

en:decreased muscle bulk

•

en:decreased mitochondrial complex iv activity (in some patients)

•

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

•

en:cox-depleted fibers

•

en:calf atrophy (later onset)

•

en:biopsy shows nonspecific myopathy without rimmed vacuoles

•

en:atrophy of the intrinsic foot and hand muscles

•

en:absence of collagen vi immunostaining

•

en:muscle biopsy shows decreased glycosylation of alpha-dystroglycan

•

en:episodic, nonerythematous, nonpruritic, nontender edema, episodic

•

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

•

en:focal lymphocytic and macrophage infiltrates on biopsy

•

en:lipohypoplasia, regional

•

en:gait unsteady

•

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

•

en:muscle atrophy (type i)

•

en:muscle biopsy shows cytochrome c oxidase-negative fibers

•

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

•

en:lymphedema of the extremities

•

en:lymphedema, dorsa of feet

•

en:lower limb muscle atrophy (in 2 of 3 families)

•

en:loss of subcutaneous fat

•

en:mitochondrial vacuolization seen on muscle biopsy

•

en:limb-girdle myopathy

•

en:hypertonia late

•

en:levator palpebrae superioris atrophy

•

en:generalized muscle wasting

•

en:hamstring muscle affected

•

en:generalized muscle contractions, episodic

•

en:head drop due to neck muscle weakness

•

en:impaired toe-walking

•

en:increased internal nuclei

•

en:increased intraabdominal fat

•

en:isolated necrotic fibers

•

en:muscle wasting, progressive

•

en:muscle stiffness or aching

•

en:muscle hypertrophy

•

en:muscle fiber atrophy, profound (rare)

•

en:muscle fatigability

•

en:muscle cramps during exercise

•

en:muscle coenzyme q deficiency

•

en:muscle biopsy shows ragged-red fibers with decreased cox activity

•

en:muscle biopsy shows increased number of endplate regions distributed over increased span of muscle fiber

•

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

•

en:muscle biopsy shows myofibrillar disruption

•

en:muscle biopsy shows merosin (156225)-positive muscle fibers

•

en:muscle biopsy shows lipid droplets

•

en:muscle biopsy shows grouped atrophy

•

en:muscle biopsy is immunopositive for merosin (156225)

•

en:muscle atrophy, distal, particularly affecting the hands muscle biopsy shows variation in fiber size

•

en:mitochondria show paracrystalline inclusions

•

en:mitochondrial dna deletions (in some patients)

•

en:muscle weakness, primarily proximal

•

en:proximal muscle weakness, less severe

•

en:muscle weakness associated with fasting or infection

•

en:rhabdomyolysis may occur

•

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

•

en:lymphography shows increased number of dilated lymphatic vessels (hyperplasia)

•

en:umbilical cord bleeding

•

en:thick palmar fascia

•

en:thenar muscle atrophy

•

en:tendinous and tuberous xanthoma

•

en:shoulder weakness

•

en:severely decreased or absent lamp2 protein

•

en:reduced muscle mass

•

en:muscular rigidity

•

en:proximal lower limb amyotrophy

•

en:prominent muscular appearance

•

en:positive staining for slow myosin heavy chain

•

en:plantar fibromatosis

•

en:painful muscle cramps

•

en:no lipodystrophy in face and neck

•

en:neurogenic changes later in disease seen on emg

•

en:myofibromatosis

•

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

•

en:distal muscle atrophy, predominantly lower limbs

•

en:lymphedema, hands (rare)

•

en:cox-negative fibers

•

en:distal leg muscle atrophy

•

en:difficulty climbing stairs, jumping, running

•

en:dermal or subcutaneous infiltrate of spindle-shaped cells arranged in a whorled pattern seen on histology

•

en:decreased muscle succinate dehydrogenase

•

en:decreased mitochondrial respiratory chain complex activity

•

en:decreased mitochondrial complex v activity

•

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

•

en:cytochrome-c oxidase deficiency

•

en:biopsy shows dystrophic changes

•

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

•

en:benign soft tissue developmental anomalies

•

en:axial hypotonia (in some patients)

•

en:atrophic muscle fibers

•

en:absence of spontaneous activity at birth (severe form)

•

en:abnormal mitochondrial proliferation

•

en:abnormal mitochondria

•

en:frequent falls

•

en:deterioration in ability to walk

•

en:distal lower limb amyotrophy

•

en:distal muscle weakness, affecting the lower limbs

•

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

•

en:hypotonia, axial, severe

•

en:limb weakness, proximal followed by distal

•

en:limb-girdle muscular dystrophy

•

en:limb-girdle muscle atrophy

•

en:internal nuclei

•

en:increased numbers of abnormally-shaped mitochondria in subsarcolemmal areas

•

en:increased intermyofibrillar and subsarcolemmal glycogen

•

en:hypotonia (untreated hypothyroidism)

•

en:hypotonia (in some patients)

•

en:hypertonicity (uncommon)

•

en:electron microscopy showed z-disk streaming

•

•

en:hang weakness

•

en:handgrip myotonia

•

en:greater soleus involvement than gastrocnemii involvement seen on mri

•

en:generalized amyotrophy

•

en:gastrocnemius and soleus muscles most affected

•

•

en:firm muscles

•

en:fiber type grouping

•

en:z-disk streaming

•

en:abnormal sarcoplasmic reticulum elements

•

en:difficulty in walking carrying large toy

•

en:myoclonic spasms

•

en:polymyositis

•

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

•

en:paralysis of the lower limbs (later)

•

en:paracrystalline inclusions

•

en:nonspecific myopathic changes seen on biopsy

•

•

en:myosin storage myopathy (in some patients)

•

en:myopathic pattern seen on emg

•

en:muscle weakness of limb

•

en:preserved heel standing

•

en:muscle weakness and atrophy may be asymmetric

•

en:muscle weakness, severe, diffuse

•

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

•

en:muscle hypertrophy (meb)

•

en:muscle biopsy shows myopathic or dystrophic changes

•

en:muscle biopsy shows myofibrillar myopathy

•

en:muscle biopsy shows fibrosis and increased connective tissue

•

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

•

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

•

en:prominent involvement of the quadriceps femoris muscles

•

en:muscle atrophy, diffuse, severe

•

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

•

en:rapid fatigue of gait

•

en:difficulty walking heel to toe

•

en:difficulty walking down hill

•

en:z-line streaming see on electron microscopy

•

en:weakness of neck muscles may occur later

•

en:vacuoles are autophagocytic

•

en:ubiquinone decreased

•

en:subsarcolemmal hyaline bodies in type 1 fibers only

•

en:sparing of small hand and finger muscles

•

en:prominent musculature

•

en:soft tissue or tendinous calcinosis may occur

•

en:small and incompletely fused muscle fibers seen on biopsy

•

en:shoulder muscle weakness

•

en:rimmed vacuoles

•

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

•

en:red-ragged fibers (2p21del)

•

en:proximal and distal muscle atrophy in lower limbs

•

en:proximal amyotrophy

•

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

•

en:finding related to ability to walk down hill

•

en:mtdna depletion seen on muscle biopsy

•

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

•

en:defects in mitochondria respiratory activities, mainly complexes i, ii, and iv

•

en:deep finger muscle weakness

•

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

•

en:decreased complex i activity (rare)

•

en:decreased coenzyme q10 levels in muscle

•

en:decreased caveolin-3 expression on muscle biopsy

•

en:cytochrome c oxidase-negative fibers

•

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

•

en:combined oxidative phosphorylation deficiency, complexes i and iv

•

en:distal muscle atrophy, predominantly affecting the lower limbs

•

en:biopsy of adipose tissue shows reduced adipocyte size

•

en:berardinelli-seip congenital lipodystrophy

•

en:atrophic fibers

•

en:adhalin deficiency seen on muscle biopsy

•

en:abnormal jitter seen on emg

•

en:'hanging' big toe

•

en:finding related to ability to walk up step

•

en:minicores or core-like regions may be present

•

en:disorganized myofilaments seen on muscle biopsy

•

en:unable to walk down step

•

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

•

en:hypertonicity of the lower limbs

•

en:merosin-positive biopsy

•

en:mild atrophy of the proximal lower limbs

•

en:marked muscular hypertrophy

•

en:lymphoscintigraphy shows impaired lymphatic uptake and drainage

•

en:lipoatrophy, generalized

•

en:limb-girdle muscle weakness

•

en:distal muscular atrophy due to peripheral neuropathy

•

en:hypotonia, infantile, severe

•

en:increased endomysial connective tissue around muscle fibers

•

en:humeroperoneal weakness and atrophy

•

en:electromyography shows myotonic discharges

•

en:dystrophic features seen on muscle biopsy

•

en:exercise intolerance (cvs+)

•

en:edema of dorsum of hands and feet

•

en:edema is present at birth and then slowly decreases

•

en:emg shows denervation

•

en:enlarged terminal cisternae of the sarcoplasmic reticulum

•

en:enteroviral dermatomyositis syndrome

•

en:exercise-induced myalgia

•

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

•

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

•

en:necrotic and atrophic fibers with centralized nuclei

•

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

•

en:myositis (in some patients)

•

en:myopathy, mild

•

en:myopathic changes seen on emg of affected muscle

•

en:muscle biopsy shows increased variation in fiber size

•

en:myopathic changes seen on emg

•

en:myopathic changes seen muscle biopsy

•

en:muscle weakness and atrophy, progressive

•

en:muscle weakness, proximal, slowly progressive

•

en:muscle weakness, congenital

•

en:muscle wasting in lower limbs

•

en:muscle hypertrophy in affected area

•

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

•

en:muscle biopsy shows nonspecific myopathic changes

•

en:normal or decreased facial and neck adipose tissue

•

en:skeletal muscle biopsy shows minor variation in fiber size

•

en:poor exercise tolerance

•

en:small rounded fibers

•

en:muscle biopsy shows fiber type variation (in some patients)

•

en:walking may be limited

•

en:type 2 fiber hypertrophy

•

en:superior rectus atrophy

•

en:subsarcolemmal lipofuscin-positive deposits

•

•

en:sparing of anterior tibialis muscle

•

en:some patients never achieve ambulation

•

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

•

en:poor head control in infancy

•

en:shortening of various muscle-tendon groups in feet

•

en:rhabdomyolysis (in some patients)

•

en:rhabdomyolysis, episodic

•

en:relative muscle weakness, especially in pelvic girdle

•

en:reduced o-mannosyl glycans on alpha-dystroglycan

•

en:quadriceps weakness

•

en:proximal muscles more often affected

•

en:protein aggregates resembling myofibrillar myopathy may be present

•

en:muscle biopsy shows glycogen accumulation in myofibrils and lysosomes

•

en:electromyogram abnormal

•

en:muscle biopsy shows dystrophic features

•

en:congophilic staining

•

en:difficulty walking, running, climbing stairs

•

en:denuded postsynaptic regions

•

en:deficiency of mitochondrial respiratory enzymes seen on muscle biopsy

•

en:decreased mitochondrial complex iii activity seen on muscle biopsy

•

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

•

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

•

en:cores extend along length of muscle fiber

•

en:cellulitis due to immunodeficiency

•

en:disorganization of the neuromuscular junction

•

en:calf hypertrophy (early in the disease)

•

en:a subset of patients develop bilateral weakness

•

en:angulated atrophic fibers

•

en:affected muscles show atrophy

•

en:z-disks with abnormal homogeneous material

•

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

•

en:absence of gamma-sarcoglycan protein

•

en:decreased exercise tolerance

•

en:difficulty walking on heels occurs prior to difficulty walking on toes

•

en:distal limb muscle atrophy, lower more than upper

•

en:muscle biopsy shows degenerating endplates and junctional folds

•

en:hypotonia, truncal and appendicular

•

en:muscle biopsy shows 'spheroid bodies' in type 1 muscle fibers

•

en:multiple mitochondrial dna (mtdna) deletions seen on muscle biopsy

•

en:mild decrease in mitochondrial respiratory chain activity

•

en:low maximum workload on exercise testing

•

en:localized cellulitis

•

•

en:increased lipid droplets and abnormal mitochondria

•

en:increased connective tissue and fat in muscles

•

en:hypotonia, mild

•

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

•

en:granular deposits in the sarcomeres

•

en:generalized muscle weakness (less common)

•

en:generalized limb muscle atrophy

•

en:focal loss of cross striations on muscle biopsy

•

en:fibromyalgia

•

en:fat accumulation in the suprabuttock area

•

en:fatty deposition

•

en:emg shows reduction of voluntary recruitment

•

en:weakness of anterior compartment tibial muscles

•

en:weakness of ankle plantar flexion

•

en:finding related to ability to walk down a slope

•

en:muscle weakness

•

en:onset of weakness in hands and feet

•

en:no muscle fiber necrosis

•

en:no facial muscle involvement

•

en:neck muscle hypoplasia

•

en:neck and proximal limb muscle myopathy

•

en:muscle weakness trunk

•

en:muscle weakness due to peripheral neuropathy

•

en:muscle biopsy shows neurogenic atrophy

•

en:pharyngeal muscle weakness

•

en:muscle biopsy shows mitochondrial paracrystalline inclusions

•

en:muscle biopsy shows lipid deposition

•

en:muscle biopsy shows fiber type disproportion

•

en:muscle biopsy shows dystrophic changes

•

en:muscle biopsy shows decreased secondary clefts

•

en:muscle atrophy (1 patient)

•

en:muscles have a woody consistency on palpation

•

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

•

en:pelvic girdle muscle atrophy

•

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

•

en:lymphedema of the lower limbs (swelling is confined to below the knees)

•

en:tendon tears

•

en:abnormal mitochondrial morphology

•

en:difficulty walking up hill

•

en:deterioration in ability to walk up stairs

•

en:weakness of all intrinsic hand muscles (later)

•

en:virtually no active movement at birth (wws)

•

en:upper limb weakness

•

en:tubular aggregates mainly in type 1 fibers

•

en:subsarcolemmal accumulations of abnormally shaped mitochondria seen with electronmicroscopy

•

en:proximal muscle weakness (85% of patients)

•

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

•

en:structurally abnormal mitochondria

•

en:small, angulated muscle fibers seen on muscle biopsy

•

en:severe muscular hypotonia

•

en:secondary myopathic features

•

en:quadriceps atrophy

•

en:pseudoathletic appearance with prominent muscles before disease onset

•

en:proximal muscle weakness more severe than distal muscle weakness

•

en:mallory-like bodies

•

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

•

en:lower limbs more affected than upper limbs

•

en:congophilic inclusions

•

en:distal atrophy of the legs

•

en:disorganization of the myofibrillar pattern

•

en:decreased muscle mass (especially in lower limbs)

•

en:decreased muscle mass

•

en:decreased mitochondrial respiratory activities (in some patients)

•

en:cox-negative fibers seen on muscle biopsy

•

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

•

en:centralized nuclei, rare

•

en:dystrophic changes occur later

•

en:buffalo hump

•

en:axial muscle hyperextension, episodic

•

en:attacks of weakness

•

en:attacks last 4 to 24 hours

•

en:atrophy of type 1 and type 2 fibers

•

•

en:limb-girdle muscle weakness (2 families)

•

en:amyloid deposition in muscle fibers occurs rarely

•

en:distal limb muscle atrophy (less common)

•

en:atrophy of neck muscles may occur later

•

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

•

en:hip flexor weakness

•

en:indentations or folds of the sarcolemma are connected to the membranes enclosing the vacuoles

•

en:inclusions are tdp43-immunoreactive

•

en:increased variability of fiber size seen on muscle biopsy

•

en:hypotonia at birth

•

en:hypotonia, severe, neonatal

•

en:hypoplastic deltoids

•

en:electron microscopy shows subsarcolemmal accumulations of abnormally shaped mitochondria

•

en:hyaline plaques with absent oxidative activity

•

en:hypoplasia of serratus anterior muscle

•

en:grip strength decreased

•

en:generalized neonatal hypotonia

•

en:gait abnormalities (occurs later)

•

en:flaccid weakness or paralysis, episodic attacks

•

en:fatty infiltration

•

en:fasciculations (less common)

•

en:extensive fatty infiltration on biopsy

•

en:episodic weakness may or may not occur independent of myotonia

•

en:emg shows neurogenic changes

•

en:muscle weakness following prolonged exercise

•

en:muscle weakness, severe, proximal and distal

•

en:muscle weakness, severe, axial and proximal predominance

•

en:muscle weakness, proximal limb muscle, mild to moderate

•

en:muscle weakness, predominantly proximal

•

en:muscle weakness, hypokalemia-related

•

en:mitochondrial dna depletion, severe

•

en:muscle weakness, distal, restricted to the lower limbs

•

en:muscle stiffness

•

en:muscle hematoma

•

en:muscle biopsy shows small nerve terminals

•

en:muscle biopsy shows myopathic changes

•

en:muscle biopsy shows decreased postsynaptic areas of clefts and folds

•

en:muscle atrophy

•

en:lower limbs more often affected

•

en:muscle weakness may affect upper limbs

•

en:shoulder muscle hypoplasia

•

en:myopathic pattern seen on emg (in some patients)

•

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

•

en:wrist swelling

•

•

en:velopharyngeal muscle weakness

•

en:upper limb involvement occurs later or not at all

•

en:upper and/or lower limbs may be affected

•

en:triceps weakness

•

en:tremor of the upper limb

•

en:symptoms may be induced by heat

•

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

•

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

•

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

•

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

•

en:proximal and distal muscle atrophy

•

en:primary myopathic changes seen on emg

•

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

•

en:nonspecific myopathic changes

•

en:myxedematous appearance

•

en:loss of antigravity strength

•

en:distal muscle atrophy due to peripheral neuropathy

•

en:limb muscle weakness and atrophy, distal, neurogenic

•

en:centrally nucleated skeletal muscle fibers

•

en:decreased amplitude of miniature endplate potentials (mepp)

•

en:decreased activity of multiple mitochondrial respiratory complex enzymes

•

en:decreased activity of mitochondrial complex iii

•

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

•

en:contractures of upper limbs (in some patients)

•

en:combined mitochondrial respiratory chain deficiency (in most patients)

•

en:chronic weakness

•

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

•

en:defective glycosylation of alpha-dystroglycan seen on biopsy

•

en:biopsy shows defects in pyruvate oxidation

•

en:atrophy of upper girdle muscles

•

en:atrophy of the muscles in the anterior compartment of the lower leg

•

en:acquired partial lipodystrophy

•

en:accumulation of abnormal mitochondria

•

en:abdominal wall muscle weakness (later onset)

•

en:muscular dystrophy, congenital, 1c

•

en:decreased muscle action potential after warming affected muscle

•

en:difficulty rising from chair

•

•

en:hypertrophy of calves (in 3 of 6 patients)

•

en:large lipid droplets

•

en:infantile muscular hypotonia

•

en:increased fat and fibrous tissue

•

en:increased fatty and connective tissue in skeletal muscle

•

en:increased connective tissue

•

en:increased centralized nuclei

•

en:increased adipose fibrosis

•

en:glycogen depletion in skeletal muscle

•

en:emg may showed myotonic discharges

•

en:glycogen accumulation seen on biopsy

•

en:foot extensor muscle weakness (later onset)

•

•

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

•

en:emg shows myopathy

•

en:emg shows myopathic or neurogenic changes

•

en:emg may show neurogenic changes

•

en:difficulty walking up step

•

en:hyporeflexia

•

en:difficulty running

•

en:myotonia is most pronounced in the extremities

•

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

•

en:proximal muscles may be mildly affected

•

en:postexercise cmap amplitude facilitation

•

en:poor head control

•

en:normal dystrophin immunostaining

•

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

•

en:nemaline bodies

•

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

•

en:relative sparing of the rectus femoris

•

en:myopathy, mild to severe

•

en:myopathic findings on biopsy have been occasionally reported

•

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

•

en:myopathic and neurogenic changes seen on emg

•

en:muscular hypotonia of the trunk

•

en:muscular dystrophy (in some patients)

•

en:muscle weakness and atrophy, proximal

•

en:proximal muscle weakness in lower limbs

•

en:rupture of muscle

•

en:muscle fibers are immunoreactive for desmin and vimentin

•

en:type 1 fiber predominance

•

en:abnormal fat accumulation in the back (in some patients)

•

en:finding related to ability to walk heel to toe

•

en:does walk on uneven surface

•

en:z-band streaming

•

en:weakness and wasting of the lower limbs

•

en:walking delay

•

en:upper limb involvement may occur later

•

en:transient neonatal hypotonia (less common)

•

en:shoulder girdle muscle atrophy

•

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

•

en:tenderness of lower extremities

•

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

•

en:subsarcolemmal mitochondrial accumulation

•

en:stiffness (uncommon)

•

en:slowly progressive limb-girdle myopathy

•

en:skeletal muscle shows decreased sarcoglycan proteins

•

en:muscle wasting, severe, primarily in the legs

•

en:reduced muscle bulk

•

en:muscle fatigue

•

en:decreased activities of several mitochondrial respiratory enzymes

•

en:exercise capacity decreased

•

en:emg may show myopathic features

•

•

en:distal muscle weakness

•

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

•

en:decreased mitochondria

•

en:decreased coenzyme q10

•

en:congenital myasthenic syndrome (reported in 1 patient who survived to age 20 years)

•

en:fiber-type grouping pattern

•

en:calf pseudohypertrophy rare

•

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

•

en:attacks precipitated by hypokalemia, administration of glucose or insulin, heavy carbohydrate consumption, stress, fatigue, rest after exercise

•

en:angulated atrophic muscle fibers

•

en:absence of some scapular muscles (less common)

•

en:muscle cramp

•

en:absence of necrosis

•

en:fat pad between achilles tendon and medial malleolus

•

en:difficulty rising from a squatting position

•

en:fiber size variation seen on muscle biopsy

•

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

•

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

•

en:muscle biopsy shows atrophy

•

en:muscle aches, intermittent

•

en:mildly decreased laminin alpha-2 expression (lama2, 156225)

•

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

•

en:muscle biopsy shows ragged red fibers

•

en:limb muscle weakness, proximal, upper and lower

•

en:lipomas or lipomatous masses (most cases)

•

en:increased connective tissue (in some patients)

•

en:inability to stand on tiptoes

•

en:inability to run

•

en:impaired heel-walking

•

en:hypoplasia of cervical paravertebral muscles

•

en:hypertrophy of the extensor digitorum brevis muscles

•

en:gluteal hypoplasia

•

en:fragmented mitochondrial network

•

en:proximal muscle weakness (120270.0002)

•

en:proximal muscle involvement may occur

•

en:polyglucosan accumulation

•

en:pelvic girdle muscle weakness (occurs earlier)

•

en:panniculitis

•

en:neonatal hypotonia

•

•

en:myofibrillar lesions

•

en:muscle atrophy (variable)

•

en:muscular dystrophy

•

en:muscle weakness (in 90% of patients)

•

en:muscle weakness (1 patient)

•

en:muscle weakness, proximal, lower limbs (upper limbs may become affected later)

•

en:muscle biopsy shows sarcoplasmic pas-positive vacuoles

•

en:muscle biopsy shows intranuclear tubulofilamentous inclusions

•

en:muscle atrophy, limb-girdle and proximal

•

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

•

en:rectus medial atrophy

•

en:walking difficulty due to multiple sites

•

en:rigidity (uncommon)

•

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

•

en:mild weakness

•

en:abnormal iron deposition in mitochondria

•

en:difficulty walking up a slope

•

en:difficulty managing stairs on all fours

•

en:difficulty initiating walking

•

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

•

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

•

en:variation of fiber size and shape

•

en:vacuolar myopathy may occur

•

en:severe form shows absence of spontaneous activity at birth

•

en:vacuolar membranes immunostain with sarcolemmal proteins

•

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

•

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

•

en:swelling of the extremities, episodic

•

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

•

en:mitochondrial dna depletion (in some)

•

en:absence of telethonin protein

•

en:mildly decreased cytochrome c oxidase activity

•

en:decreased activity of respiratory complex ii+iii

•

en:distal muscle weakness and atrophy may occur, upper and lower limbs affected

•

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

•

en:distal limb muscle weakness, lower more than upper

•

en:decreased shank muscle mass

•

en:decreased lipoic acid

•

en:decreased distal reflexes

•

en:decreased caveolae in muscle tissue

•

en:cores or minicores

•

en:dystrophic changes may be present

•

en:autophagic vacuoles with multilamellar structures seen on electron microscopy

•

en:atrophy of anterior compartment tibial muscles

•

•

en:areflexia due to muscle weakness

•

en:ankle edema (finding)

•

en:biopsy shows degenerative changes consistent with myopathy

•

en:abnormal fat distribution

•

en:'sloping' shoulders due to muscle atrophy

•

en:duchenne muscular dystrophy (dmd, 310200) in 'complex' form

•

en:dystrophic changes seen on skeletal muscle biopsy

•

en:may have proximal muscle weakness later in the disease

•

en:immunoreactivity for z-disk proteins

•

en:many fibers with internal nuclei

•

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

•

en:loss of lower-limb tendon reflexes

•

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

•

en:inguinal hernia

•

en:increased endomysial fibrosis

•

en:increased endo- and perimysial connective tissue

•

en:inability to sit or hold head up

•

en:imaging shows muscle atrophy and fatty replacement

•

en:easy fatigue

•

en:hypotonia, neonatal and later

•

en:hyporeflexia of lower limbs

•

en:hamstring and quadriceps muscles mildly affected

•

en:gowers sign (in some patients)

•

en:fibrillation

•

en:emg shows myopathic changes

•

en:emg shows fibrillation potentials

•

en:edema at birth

•

en:apoptotic nuclei

•

en:inclusion body myopathy

•

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

•

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

•

en:nemaline rods may be observed

•

en:myopathy in approximately 45% of patients

•

en:myofibrillar myopathy

•

en:muscle weakness, proximal, limb-girdle

•

en:muscle weakness, distal, particularly affecting the hands

•

en:muscle mitochondria normal by histochemical analysis

•

en:muscle cramps at rest

•

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

•

en:no staining for periodic acid schiff (pas)

•

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

•

en:muscle biopsy shows loss of myofibrillar organization

•

en:muscle biopsy shows hypotrophy of type 1 muscle fibers

•

en:muscle biopsy shows abnormal mitochondria

•

en:biopsy shows myopathic and dystrophic changes

•

•

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

•

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

•

en:nonspecific myopathy

•

en:painful swelling in aponeuroses

•

en:minicores (in some)

•

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

•

oedème de la face

•

faiblesse de muscle

•

en:walking difficulty due to lower leg

•

en:finding related to ability to walk up hill

•

en:finding related to ability to walk on the flat

•

en:finding related to ability to walk carrying large toy

•

en:does not walk

•

en:z-disk degeneration

•

en:swelling of the hands and feet, episodic

•

en:pectoralis major hypoplasia

•

en:shortening of various muscle-tendon groups in legs

•

en:rhabdomyolysis with exercise (in older patients)

•

en:ragged-red muscle fibers

•

en:ragged-red fibers on muscle biopsy

•

en:proximal weakness

•

en:proximal muscle weakness, limb-girdle distribution

•

en:peroneal muscle atrophy

•

en:pelvic muscle involvement occurs later

•

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

•

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

•

en:mild weakness of the small hand muscles

•

en:decreased muscle mitochondrial aconitase

•

en:distal muscle atrophy due to neuropathy

•

en:distal limb muscle weakness occurs later

•

en:mild variability in muscle fiber size

•

en:difficulty walking and climbing stairs

•

en:deltoid muscle hypoplasia

•

en:delayed motor development (cvs+)

•

en:degenerating nerve terminals

•

en:decreased expression of the vdac1 protein

•

en:distal muscle weakness, predominantly lower limbs

•

en:decreased activity of cytochrome c oxidase (in most cases)

•

en:deafferentation

•

en:congophilic deposits

•

en:chronic denervation seen on skeletal muscle biopsy

•

en:central cores seen on muscle biopsy

•

en:calf muscle hypertrophy

•

en:calf hypertrophy (reported in 1 family)

•

en:calcific tendinopathy, early-onset (in some patients)

•

en:distal muscle wasting, mild

•

en:distal limb atrophy (upper and lower)

•

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

•

en:hypoplasia of latissimus dorsi muscle

•

en:loss of independent ambulation around age 12 years

•

en:loss of adipose tissue occurs around puberty

•

en:lipodystrophy, generalized, panniculitis-induced (in some)

•

en:distal muscle weakness due to peripheral neuropathy

•

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

•

en:increased muscle tone (early in life)

•

en:increased fatty infiltration

•

en:increased central nucleation

•

en:knee and hip flexor weakness due to peripheral neuropathy

•

•

•

en:foot dorsiflexor weakness

•

en:emg shows myopathic features

•

en:emg in myotonia permanens shows continuous myotonic activity

•

en:emg - repetitive muscle discharges

•

en:electromyogram normal

•

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

•

en:gowers sign present

•

en:trunk muscle atrophy

•

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

•

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

•

en:small or absent axon terminals

•

•

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

•

en:tubular aggregates seen on biopsy

•

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

•

en:umbilical depression

•

en:variation of myofiber diameter

•

en:miyoshi muscular dystrophy 3

•

en:shoulder girdle weakness

◀

• Mathieu Lafourcade • LIRMM (données libres en Creative Commons - C0 domaine public) •

• This page link : https://www.jeuxdemots.org/diko.php?gotermid=7119540 • caches: c1=8 c2=1003 c3=1

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