Le Diko - en:mitochondrial vacuolization seen on muscle biopsy

waiting

Le Diko - en:mitochondrial vacuolization seen on muscle biopsy

Javascript doit fonctionner ! Activez-le et rechargez cette page.

le dictionnaire d'associations lexicales
contributif et libre de JeuxDeMots

en:mitochondrial vacuolization seen on muscle biopsy

Nom

Informations lexicales

Langue:anglais

Associations d'idées

1000

en:muscle weakness, proximal, limb-girdle

•

en:neurogenic changes seen on emg and biopsy

•

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

•

en:angulated fibers

•

en:congenital muscular dystrophy (disorder)

•

en:decreased muscle mass (especially of limbs)

•

en:muscle biopsy shows degenerating endplates and junctional folds

•

en:muscle biopsy shows necrotic and atrophic fibers with centralized nuclei

•

en:proximal muscle weakness occurs later

•

en:abnormal iron deposition in mitochondria

•

en:calf muscle hypertrophy

•

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:emg shows myopathic or neurogenic changes

•

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

•

en:superior rectus atrophy

•

en:abnormal axons with sprouting and swelling

•

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

•

en:muscle biopsy shows myofibrillar disruption

•

en:myogenic changes seen on emg

•

en:painful swelling in fasciae

•

en:cytoplasmic inclusion bodies (finding)

•

en:calf muscle discomfort

•

en:muscle biopsy shows fiber type disproportion

•

en:neck muscle hypoplasia

•

en:shoulder weakness and atrophy

•

en:upper limb weakness

•

en:z-disk degeneration

•

en:vacuoles are autophagocytic

•

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

•

en:biopsy muscle normal

•

en:calf muscle weakness

•

en:cores or minicores

•

en:emg shows denervation

•

en:enlarged mitochondria

•

en:exertional fatigue

•

en:mitochondria show paracrystalline inclusions

•

en:muscle biopsy shows glycogen accumulation in myofibrils and lysosomes

•

en:myopathic changes seen muscle biopsy

•

en:plantar fibromatosis

•

en:atrophy of neck muscles may occur later

•

en:difficulty rising from a squatting position

•

en:edematous hands and feet (1 patient)

•

en:facial muscle atrophy of involved side

•

en:replacement of affected muscle tissue with fatty tissue

•

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

•

•

en:weakness of all intrinsic hand muscles (later)

•

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

•

en:distal muscle atrophy (1 patient)

•

en:forearm muscle weakness

•

en:increased internal nuclei

•

en:marked muscular hypertrophy

•

en:muscle mounding

•

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

•

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

•

en:large lipid droplets

•

en:minicore-like lesions with mitochondrial depletion and sarcomeric disorganization

•

en:myopathic pattern seen on emg

•

en:normal or increased truncal adipose tissue

•

en:proximal weakness

•

en:quadriceps atrophy

•

en:fatty deposition

•

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

•

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

•

en:absence of merosin in muscle

•

en:amyotrophy affects c5 to t1 myotomes

•

en:increased connective tissue (in some patients)

•

en:limb muscular atrophy

•

en:muscle pain (less common)

•

en:muscle wasting in lower limbs

•

en:hip girdle muscle atrophy

•

en:decreased mitochondrial respiratory activities (in some patients)

•

en:fasciculations (in some patients)

•

•

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

•

en:muscle biopsy shows preserved junctional folds

•

en:myofibrillar disorganization

•

en:transient neonatal hypotonia (less common)

•

en:no dystrophic changes

•

en:muscle weakness, hypokalemia-related

•

en:increased muscle tone at birth

•

en:loss of facial adipose tissue

•

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

•

en:hypertrophy of the extensor digitorum brevis muscles

•

en:cold sensitivity has been reported

•

en:'hanging' big toe

•

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

•

en:decreased mtdna

•

en:edema at birth

•

en:inability to jump or squat

•

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

•

en:preserved heel standing

•

en:myotonia is usually not seen

•

en:distal muscle weakness due to neuropathy

•

en:type ii fiber atrophy seen on muscle biopsy

•

en:muscle fiber atrophy, profound (rare)

•

en:myopathy with abnormal lipid metabolism

•

en:increased subcutaneous truncal adipose tissue

•

en:weakness may be exacerbated by illness or stress

•

en:emg shows fasciculations

•

en:muscle mitochondria normal by histochemical analysis

•

en:muscle stiffness (in older patients)

•

en:increased fiber size variability

•

en:limb-girdle muscle weakness (2 families)

•

en:inflammatory cells absent

•

en:minicores or core-like regions may be present

•

en:difficulty raising arms

•

en:acquired partial lipodystrophy

•

en:absence of myotonia in infancy (congenital form)

•

en:loss of subcutaneous fat, particularly affecting the limbs

•

en:muscle weakness and atrophy, proximal

•

en:rectus medial atrophy

•

en:chronic denervation seen on skeletal muscle biopsy

•

en:emg may showed myotonic discharges

•

en:hand muscle atrophy

•

en:muscle atrophy (type i)

•

en:muscle biopsy shows neurogenic changes

•

en:muscle weakness (in some patients)

•

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

•

en:adhalin deficiency seen on muscle biopsy

•

en:muscle biopsy shows core-like regions devoid of oxidative activity

•

en:muscle biopsy is immunopositive for merosin (156225)

•

en:muscle biopsy may show inflammatory changes

•

en:muscle cramps during exercise

•

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

•

en:muscle biopsy shows type 2 fiber atrophy (see details under neurologic heading)

•

en:mri shows fatty infiltration of affected muscles

•

en:multi-core congenital myopathy

•

en:involves upper and lower proximal muscles

•

en:marked lack of adipose tissue

•

en:lymphoscintigraphy shows impaired lymphatic uptake and drainage

•

en:lymphedema of the extremities

•

en:lipomas or lipomatous masses (most cases)

•

en:muscle weakness, proximal, due to neuronopathy begins in the lower limbs and then progresses to upper limbs

•

en:increased muscle tone in the lower limbs

•

en:inclusions show positive immunostaining for sqstm1 and ubiquitin

•

en:inability to stand on tiptoes

•

en:hypotrophy of type 1 fibers

•

en:muscle fibers appear as fetal myotubules

•

en:nemaline rods (rare)

•

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

•

en:proximal upper limb amyotrophy

•

en:thickening of fascia of forearm

•

en:subcutaneous edema

•

•

en:soft fleshy palms (50%)

•

en:relative muscle weakness, especially in pelvic girdle

•

en:redundancy of basal lamina with accumulated debris

•

en:ragged-red fibers seen on muscle biopsy

•

en:quadriceps atrophy (later onset)

•

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

•

en:muscle weakness, upper and lower limbs

•

en:progression to wheelchair in fourth decade

•

en:predominantly lower limb lymphedema

•

en:poor exercise tolerance

•

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

•

en:partial lipodystrophy (abnormal distribution of adipose tissue)

•

en:nonspecific myopathic changes

•

en:hypoplasia of serratus anterior muscle

•

en:myxedematous appearance

•

en:muscular rigidity

•

en:hypotonia at birth

•

en:fatty infiltration seen on muscle biopsy

•

•

en:benign soft tissue developmental anomalies

•

en:decreased activity of multiple mitochondrial respiratory complex enzymes

•

en:decreased ability to run

•

en:cranial muscles spared

•

en:congophilic eosinophilic inclusions

•

en:calf hypertrophy (uncommon)

•

en:calf and thigh cramping muscle pains

•

en:biopsy shows myopathy without vacuoles

•

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

•

en:axial hypotonia (in some patients)

•

en:decreased coenzyme q10 content

•

en:atrophy of shins

•

en:atrophy, neurogenic muscular

•

en:ascites (in some patients)

•

en:angulated atrophic fibers

•

en:amorphous granulofilamentous material associated with z-discs

•

en:abnormal fat distribution

•

en:abnormal aggregates of desmin and filamin c

•

en:umbilical cord bleeding

•

en:decreased amplitude of miniature endplate potentials (mepp)

•

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

•

en:gluteal hypoplasia

•

en:dystrophic changes seen on muscle biopsy

•

en:foot dorsiflexor weakness

•

en:fiber-type grouping pattern

•

en:fatty infiltration

•

en:fasciculations (less common)

•

en:fasciculation

•

•

en:edema (hands and feet)

•

en:dystrophic features

•

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

•

en:decreased lipoic acid

•

en:distal muscle atrophy due to denervation

•

en:difficulty standing

•

en:denervation of skeletal muscles

•

en:delayed ambulation

•

en:defects in lipoate-containing mitochondrial enzyme complexes

•

en:decreased thiamine pyrophosphate

•

en:decreased muscle succinate dehydrogenase

•

en:decreased mitochondrial respiratory chain complex activity

•

en:decreased mitochondrial complex iii activity seen on muscle biopsy

•

en:type 1 fibers with inclusions containing myh7 protein aggregates

•

en:decreased cytochrome c oxidase staining

•

en:umbilical hernia

•

en:muscle weakness is not a feature

•

en:pelvic girdle weakness

•

en:pelvic girdle muscle atrophy

•

en:pectoralis major hypoplasia

•

en:nemaline rods may be observed

•

en:necrotic fibers

•

•

en:myopathic findings on biopsy have been occasionally reported

•

en:muscle weakness of limb

•

en:muscle weakness, variable

•

en:proximal muscles may be mildly affected

•

en:muscle weakness, symmetric, proximal, lower limbs

•

en:muscle weakness, mild, proximal and distal

•

en:muscle strength and bulk is preserved

•

en:muscle paralysis, episodic

•

en:muscle hypertrophy (meb)

•

en:muscle fiber necrosis

•

en:muscle biopsy shows type 1 fiber predominance

•

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

•

en:protein aggregates immunopositive for actin and desmin

•

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

•

en:muscle biopsy shows chronic and active denervation

•

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

•

en:variable deficiencies of mitochondrial respiratory chain enzymes

•

en:ubiquinone decreased

•

en:type 2 fiber atrophy see on biopsy

•

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

•

en:tubulofilamentous inclusions

•

en:trunk muscle atrophy

•

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

•

en:swelling of the affected areas

•

en:stiffness (uncommon)

•

en:ragged red fibers seen on biopsy

•

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

•

en:some patients become wheelchair-dependent

•

en:slim, muscular build (in some patients)

•

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

•

en:severe muscle hypotonia at birth

•

en:secondary loss of sarcolemmal caveolin-3

•

en:sarcoplasmic accumulation of electron-dense granulofilamentous material

•

en:reduced subcutaneous adipose tissue

•

en:recovery between attacks

•

en:muscle biopsy shows decreased or absent dysferlin staining

•

en:polymyositis

•

en:muscle atrophy, mild

•

en:calf muscle pseudohypertrophy

•

en:disruption plasma membrane (in some patients)

•

en:disruption of the m-line

•

en:dense membranous structure surrounding nuclei on electron microscopy

•

en:decreased levels and activity of mitochondrial respiratory complexes i and iv

•

en:decreased coenzyme q10 levels in muscle

•

en:decreased adipose tissue around neck

•

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

•

en:congenital fiber-type disproportion

•

en:biopsy shows nonspecific myopathy without rimmed vacuoles

•

en:distal muscle atrophy due to neurologic disease

•

en:biopsy shows myopathic and dystrophic changes

•

en:axial weakness

•

en:autophagosome

•

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

•

en:accumulation of intrasarcoplasmic granulofilamentous aggregates that are immunoreactive to desmin and alpha-beta-crystallin

•

en:absence of muscle pseudohypertrophy

•

en:abnormal fat accumulation below the triceps (in some patients)

•

en:muscle amyotrophy

•

en:walking may be limited

•

en:distal limb muscle atrophy, lower more than upper

•

en:decreased activity of mitochondrial respiratory complexes i, iii, and iv in muscle tissue

•

en:distal muscle weakness and atrophy

•

en:greater soleus involvement than gastrocnemii involvement seen on mri

•

en:mitochondria dna deletion

•

en:distal myopathy (in 1 family)

•

en:lipodystrophy (in some patients)

•

en:increased mitochondria with rare paracrystalline inclusions

•

en:increased fat and fibrous tissue

•

en:increased adipose fibrosis

•

en:impaired mitochondrial respiration

•

en:hypoactive gag reflex

•

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

•

en:mitochondrial myopathy, severe

•

en:generalized weakness (adult-onset)

•

en:dystrophic changes on biopsy

•

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

•

en:dystrophic changes

•

•

en:emg may show neurogenic changes

•

en:emg shows fibrillation potentials

•

en:fetal akinesia deformation sequence

•

en:myopathy, nonprogressive

•

en:muscle fatigability

•

en:muscle weakness (in 90% of patients)

•

en:muscle weakness (1 patient)

•

en:muscle weakness, severe, proximal and distal

•

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

•

en:muscle wasting, progressive

•

en:muscle fiber splitting (in some patients)

•

en:muscle fibers contain internal nuclei

•

en:muscle atrophy (variable)

•

en:muscle biopsy shows neurogenic atrophy affecting both fibers types

•

en:muscle biopsy shows mitochondrial aggregates

•

en:muscle biopsy shows hypoglycosylation of alpha-dystroglycan

•

en:motor developmental delay

•

en:lipoatrophy of trunk

•

en:mitochondria are placed at the periphery of muscle fibers

•

en:mitochondrial dna deletion (1 patient)

•

en:lipohypoplasia, regional

•

en:myotonia is present in majority of cases

•

en:myotonia (delayed muscle relaxation after contraction)

•

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

•

en:necrotic and atrophic fibers with centralized nuclei

•

en:skeletal muscle biopsy shows reducing bodies

•

en:lipid droplet accumulation

•

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

•

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

•

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

•

en:type 1 muscle fiber predominance

•

en:tubular aggregates (in some patients)

•

en:swelling of the extremities, episodic

•

en:subsarcolemmal lipofuscin-positive deposits

•

en:shortening of flexor profundus muscle-tendon unit

•

en:neonatal hypotonia

•

en:secondary loss of merosin and desmin

•

en:relative sparing of the tibialis anterior

•

en:rectus abdominis muscle separation

•

en:proximal muscle involvement may occur

•

en:proximal lower limb amyotrophy

•

en:positive staining for atpase activity at ph of 4.3

•

en:normal muscle fiber (hcs)

•

en:neuropathic process seen on muscle biopsy

•

en:neurogenic changes later in disease seen on emg

•

en:lipoatrophy, generalized

•

en:autophagic rimmed vacuoles

•

en:limb weakness and atrophy

•

en:difficulty running and jumping

•

en:emg shows chronic denervation

•

en:emg may show myopathic features

•

en:electromyography shows myotonic discharges

•

en:edema of dorsum of hands and feet

•

en:edema, subcutaneous, generalized

•

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

•

en:distal lower limb anterior compartment weakness

•

en:difficulty walking, running, climbing stairs

•

en:difficulty climbing stairs, jumping, running

•

en:emg shows myopathic pattern

•

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

•

en:defective glycosylation of alpha-dystroglycan seen on biopsy

•

en:decreased caveolae in muscle tissue

•

en:decreased activities of mitochondrial-encoded respiratory chain complexes

•

en:cox-deficient fibers

•

en:coenzyme q10 deficiency

•

en:calf muscle enlargement

•

en:ankle clonus

•

en:acute rhabdomyolysis

•

en:emg shows myopathic and neurogenic changes

•

en:emg shows neurogenic changes

•

en:limb-girdle myopathy

•

en:hypoplastic deltoids

•

en:limb-girdle muscle weakness

•

en:lack of facial subcutaneous fat

•

en:knee and hip flexor weakness due to peripheral neuropathy

•

en:increased lysosomal glycogen

•

en:increased intraabdominal fat

•

en:increased focal mitochondrial density

•

en:increased fatty infiltration

•

en:increased central nucleation

•

en:hypotonia, fixed

•

en:hip girdle muscle weakness (usually presenting symptom)

•

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

•

en:head drop due to neck muscle weakness

•

en:grip strength decreased

•

en:glycogenosis of skeletal muscle, mild (in some patients)

•

en:generalized muscle weakness also seen in symptomatic carrier females

•

en:gait unsteady

•

en:fiber type variation seen on biopsy

•

en:fat pads on the hands and feet

•

en:exercise-induced myalgia

•

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

•

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

•

en:cores contain densely packed myofilaments

•

en:asymmetric muscle involvement

•

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

•

en:neonatal hypertonias

•

en:myotonic discharges

•

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

•

en:muscle weakness, severe, diffuse

•

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

•

en:muscle wasting due to chronic denervation

•

en:muscle hypertrophy may occur

•

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

•

en:muscle biopsy shows necrotic and regenerating fibers

•

en:nonspecific myopathic changes seen on biopsy

•

en:muscle biopsy shows loss of myofibrillar organization

•

en:muscle biopsy shows lipid deposition

•

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

•

en:muscle biopsy shows atrophy

•

en:muscle atrophy restricted to the upper limb

•

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

•

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

•

en:mitochondrial swelling

•

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

•

en:nonspecific muscle fiber atrophy

•

en:nonspecific myopathy

•

en:lower limb muscle hypotrophy

•

en:thickened subcutaneous tissue

•

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

•

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

•

en:weakness of ankle plantar flexion

•

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

•

en:upper limb muscle hypoplasia

•

en:type 1 fiber atrophy

•

en:tubulofilamentous nuclear or cytoplasmic inclusions on biopsy

•

en:biceps brachii atrophy

•

en:swelling of the hands and feet, episodic

•

en:normal sensation

•

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

•

en:structurally abnormal mitochondria

•

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

•

en:reduced muscle tone but normal power

•

en:proximal muscle weakness, mild

•

en:proximal muscle weakness

•

en:predominance of oxidative fibers

•

en:patients achieve independent ambulation, but may lose it

•

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

•

en:mildly decreased cytochrome c oxidase activity

•

en:tubular aggregates mainly in type 1 fibers

•

en:loss of subcutaneous and visceral adipose tissue, mild

•

en:decreased immunostaining for alpha-sarcoglycan

•

en:distal leg muscle atrophy

•

en:distal amyotrophy (hands and feet)

•

en:deposits immunoreactive to beta-amyloid protein

•

en:delayed motor development (cvs+)

•

en:defective mitochondrial oxidative phosphorylation of multiple enzymes

•

en:deep finger muscle weakness

•

en:decreased shoulder muscle mass

•

en:decreased or patchy amounts of alpha-dystrobrevin and beta-2-syntrophin at the sarcolemma

•

en:decreased glycosylation of alpha-dystroglycan

•

en:distal muscle weakness, predominantly affecting the lower limbs

•

en:decreased expression of the vdac1 protein

•

en:decreased activity of mitochondrial complex i

•

en:cox-negative fibers seen on muscle biopsy

•

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

•

en:calf pseudohypertrophy rare

•

en:calf hypertrophy (in some patients)

•

en:biopsy shows degenerative changes consistent with myopathy

•

en:biopsy of adipose tissue shows reduced adipocyte size

•

en:loss of ability to walk in early childhood

•

en:distal limb muscle atrophy due to peripheral neuropathy

•

en:congophilic deposits

•

en:dystrophic features and atrophic fibers seen on muscle biopsy

•

en:histochemically normal type-ii muscle fibers

•

en:localized cellulitis

•

en:easy fatigability

•

en:lipodystrophy

•

en:lipoatrophic appearance

•

en:infantile muscular hypotonia

•

en:increased perisarcolemmal calcium deposition

•

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

•

en:inability to sit or hold head up

•

en:hypoplasia of infraspinatus muscle

•

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

•

•

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

•

en:hang weakness

•

en:electromyographic decrements in some muscles

•

en:electromyogram abnormal

•

en:electron microscopy showed z-disk streaming

•

en:easy fatigue

•

en:facial muscle weakness and atrophy, progressive

•

en:fatty replacement

•

en:granular deposits in the sarcomeres

•

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

•

en:patchy muscle fiber degeneration

•

en:no ragged-red fibers

•

en:no lipodystrophy in face and neck

•

en:normal or increased facial and neck adipose tissue

•

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

•

en:neurogenic atrophy seen on muscle biopsy

•

en:myalgia (in some patients)

•

en:nemaline bodies (rods) on gomori trichrome staining

•

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

•

en:myopathy, mild

•

en:muscle weakness and atrophy, upper and lower limbs

•

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

•

en:muscle stiffness or aching

•

en:poor musculature

•

en:muscle shows lipid accumulation

•

en:phagocytic vacuoles with degraded membranous material

•

en:tubular aggregates in type 2 skeletal muscle fibers

•

en:prominent veins, lower limbs

•

en:variability in fiber size

•

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

•

en:muscle soft, tissue

•

en:z-disk streaming

•

en:wide variation in fiber size

•

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

•

en:waddling gait

•

en:tubular aggregates seen on muscle biopsy

•

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

•

en:symptoms may be induced by heat

•

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

•

en:sparing of anterior tibialis muscle

•

en:small rounded fibers

•

en:rigidity (uncommon)

•

en:rhabdomyolysis (in some patients)

•

en:rhabdomyolysis, episodic

•

en:muscle hypertrophy of the lower extremities

•

en:edema reoccurs with infections

•

en:muscle biopsy shows dystrophic features

•

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

•

en:dorsal and flexor muscles of the forearm are involved

•

en:distal limb muscular weakness due to peripheral neuropathy

•

en:denuded postsynaptic regions

•

en:defect in glycosylation of alpha-dystroglycan seen on skeletal muscle biopsy

•

en:decremental response on 3-hz repetitive nerve stimulation

•

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

•

en:cytochrome-c oxidase deficiency

•

en:emg shows myotonic changes

•

en:congenital absence of gluteal muscles

•

en:broad-based gait

•

en:atrophic calf muscles

•

en:alimentary edema

•

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

•

en:abnormal mitochondria

•

en:abnormal distribution of subcutaneous fat

•

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

•

en:emg shows spontaneous, repetitive electrical activity ('myotonic runs')

•

en:mitochondrial complex i deficiency

•

en:increased centralized internal nuclei

•

en:mild muscle weakness

•

en:merosin-positive biopsy

•

en:lymphedema of lower extremity

•

en:lymphedema, dorsa of feet

•

en:intermyofibrillar and subsarcolemmal granulofilamentous protein aggregates

•

en:increased numbers of type 1 fibers

•

en:increased muscle glycogen content

•

en:hand and foot weakness

•

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

•

en:glycogen deficiency in muscle fibers

•

en:generalized neonatal hypotonia

•

en:frontalis muscle weakness

•

en:focal areas of z-band disarray devoid of mitochondria seen on electron microscopy

•

en:finger and wrist extensor weakness

•

en:abnormal z bands

•

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

•

en:abnormal aggregation of mitochondria

•

en:neck and proximal limb muscle myopathy

•

en:absence of necrosis

•

en:muscle biopsy shows mild dystrophic changes

•

en:nemaline bodies are usually subsarcolemmal or sarcoplasmic

•

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

•

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

•

en:myalgia, episodic

•

en:muscle weakness increases with age

•

en:muscle mri shows fatty infiltration

•

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

•

en:non-pitting edema

•

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

•

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

•

en:muscle biopsy shows abnormal mitochondria

•

en:muscle aches, intermittent

•

en:muscles have a woody consistency on palpation

•

en:multiple mitochondrial dna deletions

•

en:lower limb muscle atrophy

•

en:neuropathic or myopathic changes seen on emg

•

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

•

en:lipid droplets seen on muscle biopsy

•

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

•

en:absence of some scapular muscles (less common)

•

en:z-band streaming

•

en:weakness and wasting of the lower limbs

•

en:virtually no active movement at birth (wws)

•

en:vacuolar degeneration

•

en:type ii fiber predominance

•

en:subsarcolemmal mitochondrial accumulation

•

en:postexercise cmap amplitude facilitation

•

en:skeletal muscle weakness

•

en:shoulder girdle weakness

•

en:shortening of various muscle-tendon groups in legs

•

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

•

en:severe muscular hypotonia

•

en:relatively preserved limb strength

•

en:premature exertional muscle weakness

•

en:loss of ambulation (in some patients)

•

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

•

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

•

en:berardinelli-seip congenital lipodystrophy

•

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

•

en:decreased activities of several mitochondrial respiratory enzymes

•

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

•

en:congenital, nonprogressive myopathy

•

en:increased visceral fat

•

en:bilateral foot drop

•

en:attacks of weakness

•

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

•

en:atrophy, mild (in some cases)

•

en:atrophic fibers

•

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

•

•

en:amyotrophy, neurogenic

•

en:acetazolamide may worsen symptoms

•

en:accumulated lipid droplets seen on muscle biopsy

•

en:distal muscle weakness, mild

•

en:centrally located nuclei seen on muscle biopsy

•

en:distal muscle weakness in lower limbs, severe

•

en:hypertonicity (uncommon)

•

en:increased muscle lipid content

•

en:increased glycogen

•

en:dystrophic changes seen on skeletal muscle biopsy

•

en:increased fibrosis

•

en:increased endomysial fibrosis

•

en:inclusions stain positively with nitroblue tetrazolium (nbt)

•

en:hypotonia, truncal and appendicular

•

en:hypotonia (in some patients)

•

en:hypertonia at birth

•

en:hamstring and quadriceps muscles mildly affected

•

en:glycogen accumulation seen on biopsy

•

en:gastrocnemius and soleus muscles most affected

•

en:fibrillation

•

en:fat accumulation in the suprabuttock area

•

en:episodic, nonpruritic, nonurticarial, nonpitting edema

•

en:easily fatigued (finding)

•

en:muscle weakness, proximal and distal

•

en:myotonia, cold-sensitive, predominantly of face, tongue, forearm, and hand precipitated by muscle cooling or cold exposure or rest after exercise

•

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

•

en:myopathic features seen on biopsy

•

en:myofibrillar lesions

•

en:myofibrillar disintegration

•

en:muscle atrophy, mild, more proximal than distal

•

en:muscle stiffness

•

en:muscle pain and cramping on exertion

•

en:muscle cramps, painful, recurrent

•

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

•

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

•

en:muscle biopsy shows decreased numbers of acetylcholine receptors (achr) in the postsynaptic membrane (less than 50% of normal)

•

en:muscle atrophy appears later in disease course

•

en:myotonia seen on emg

•

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

•

en:necrotic process

•

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

•

en:mitochondrial myopathy

•

en:usually a unilateral disorder

•

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

•

en:tetanus-like muscle contractions

•

en:tendinous and tuberous xanthoma

•

en:signs of denervation seen on biopsy

•

en:secondary myopathic changes

•

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

•

en:rimmed vacuoles on biopsy

•

en:reduced o-mannosyl glycans on alpha-dystroglycan

•

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

•

en:positive staining for slow myosin heavy chain

•

en:percussion myotonias

•

en:nuclear clumps

•

en:normal or decreased facial and neck adipose tissue

•

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

•

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

•

en:mild weakness of the small hand muscles

•

en:carpopedal spasm

•

en:disorganization of the myofibrillar pattern

•

en:degenerating fibers

•

en:decreased collagen vi

•

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

•

en:centrally nucleated skeletal muscle fibers

•

en:centralized myonuclei

•

en:calf hypertrophy (early in the disease)

•

en:distal limb atrophy (upper and lower)

•

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

•

en:attacks precipitated by cold temperature

•

en:atrophy of anterior compartment tibial muscles

•

en:absence of pectoralis minor muscle

•

en:absence of caveolin-3 staining

•

en:abnormal jitter seen on emg

•

en:disruption of sarcomeres with disorganization of the z band

•

en:distal lower limb muscle weakness and atrophy

•

en:mild variability in muscle fiber size

•

en:hypotonia, mild (1 patient)

•

en:marked variability of fiber size

•

en:mallory-like bodies

•

en:loss of independent ambulation around age 12 years

•

en:limb muscle weakness, proximal, upper and lower

•

en:imaging shows progressive fatty infiltration of muscle

•

en:hypotonia (cvs+)

•

en:hyporeflexia in affected muscles

•

en:easy bruisability of lower extremities

•

en:hypoplasia of cervical paravertebral muscles

•

en:humeroperoneal weakness and atrophy

•

en:heterotopic bone formation in subcutaneous fat

•

en:fibrillations in affected muscles

•

en:facial muscle atrophy

•

en:electron microscopy shows subsarcolemmal accumulations of abnormally shaped mitochondria

•

•

en:weakness of anterior compartment tibial muscles

•

en:ambulation difficulty

•

en:myalgia with febrile episodes (rare)

•

en:muscle cramps may affect jaw muscles

•

en:muscular hypotonia of the trunk

•

en:muscle weakness and atrophy, distal

•

en:muscle weakness

•

en:muscle hyperirritability

•

en:muscle fiber splitting and fibrosis seen on muscle biopsy

•

en:muscle fibers are immunoreactive for desmin and vimentin

•

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

•

en:necrotic and regenerating muscle fibers

•

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

•

en:muscle biopsy shows hypotrophy of type 1 muscle fibers

•

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

•

en:minicores extend full fiber diameter

•

en:mildly reduced respiratory enzyme activities except for complex ii

•

en:limb-girdle muscular dystrophy

•

en:myotonia is most pronounced in the extremities

•

en:neurogenic abnormalities seen on emg

•

en:increased variability in muscle fiber diameter

•

en:respiratory distress (congenital form)

•

en:umbilical depression

•

en:areflexia of lower limbs

•

en:tubular aggregates seen on biopsy

•

en:tenderness of lower extremities

•

en:shoulder girdle muscle atrophy

•

en:rimmed vacuoles with basophilic granular material

•

en:reduced muscle bulk

•

en:paralysis of the lower limbs (later)

•

en:red-ragged fibers (2p21del)

•

en:ragged-red muscle fibers

•

en:ragged-red fibers on muscle biopsy

•

en:proximal muscle weakness (85% of patients)

•

en:proximal amyotrophy

•

en:poor sarcomeric structure (in some patients)

•

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

•

en:limb-girdle muscle atrophy

•

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

•

en:increased mitochondria seen on muscle biopsy

•

en:decreased postsynaptic length

•

en:disorganization of the neuromuscular junction

•

en:difficulty running or inability to run

•

en:diastasis recti

•

en:degenerate mitochondrial on em

•

en:increased lipid droplets and abnormal mitochondria

•

en:decremental response to repetitive stimulation at neuromuscular junction

•

en:decreased muscle bulk

•

en:distal muscle weakness, affecting the lower limbs

•

en:decreased endplate potential and amplitudes

•

en:decreased acetylcholine receptors (achr) at endplate junctional folds (less common)

•

en:deafferentation

•

en:cox-depleted fibers

•

en:casq1-immunopositive inclusions

•

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

•

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

•

en:distal limb muscle weakness and atrophy

•

en:deficiency of mitochondrial complexes i, iii, and iv

•

•

en:focal loss of cross striations on muscle biopsy

•

en:increased fatty and connective tissue in skeletal muscle

•

en:hypotonia, axial, severe

•

en:edema of lower extremity

•

en:hyaline inclusion

•

en:gowers sign (in some patients)

•

en:generalized muscle weakness

•

en:generalized amyotrophy

•

en:firm muscles

•

en:fibromyalgia

•

en:facial diplegia

•

en:exercise intolerance (less common)

•

en:evidence of lymphatic rerouting

•

en:endomysial fibrosis

•

en:emg shows reduction of voluntary recruitment

•

en:nemaline bodies occur in type 1 fibers

•

en:polyglucosan accumulation

•

en:percussion-induced muscle mounding (muscle rippling)

•

en:potassium sensitivity has been reported

•

en:other mitochondrial complex enzyme activities may also be decreased

•

en:no staining for oxidative enzymes

•

en:normal phosphorylase kinase activity in muscle

•

en:muscle hypertrophy in affected area

•

en:necrotic change

•

en:myopathic changes seen on emg

•

en:myofibromatosis

•

en:muscle weakness of proximal and distal upper and lower limbs

•

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

•

en:muscle pain with exercise (in older patients)

•

en:progressive interictal weakness is common

•

en:muscle biopsy shows type 1 fiber predominance and hypertrophy

•

en:presynaptic defect at the neuromuscular junction

•

en:variation of fiber size and shape

•

en:proximal muscles more often affected

•

en:subcutaneous lipomatous tissue

•

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

•

en:upper and/or lower limbs may be affected

•

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

•

en:triceps weakness

•

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

•

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

•

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

•

•

en:proximal muscle weakness in upper limbs

•

en:skeletal muscle biopsy shows decreased cytochrome c oxidase activity

•

en:shoulder weakness

•

en:shortening of various muscle-tendon groups in feet

•

en:rhabdomyolysis may occur

•

en:retroperitoneal fibrosis (rare)

•

en:replacement of myofibers with connective tissue

•

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

•

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

•

en:absence of telethonin protein

•

en:muscle biopsy shows enlargement of type i muscle fibers, consistent with denervation

•

en:contractures of upper limbs (in some patients)

•

en:exercise intolerance (cvs+)

•

en:exercise capacity decreased

•

en:distal muscle weakness, predominantly lower limbs

•

en:distal limb muscle atrophy (less common)

•

en:decreased exercise tolerance

•

en:decreased activity of complex i and complex iv

•

en:complex v deficiency

•

en:generalized muscle weakness, proximal and distal

•

en:chronic denervation seen on emg

•

en:attacks precipitated by potassium

•

en:atrophy of the thenar and hypothenar muscles

•

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

•

en:amyotrophy, distal, upper and lower limbs

•

en:abnormal subcutaneous fat tissue distribution

•

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

•

en:flaccid weakness or paralysis, episodic attacks

•

en:hypoglycosylation of alpha-dystroglycan

•

en:muscle biopsy shows disruption of the sarcolemmal membrane

•

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

•

en:muscle biopsy shows decreased activity of cytochrome c oxidase

•

en:muscle atrophy (in some patients)

•

en:muscle atrophy, progressive

•

en:muscle activity is electrically silent on emg

•

en:multiple mitochondrial respiratory enzymes deficiencies seen on biopsy

•

en:mitochondrial paracrystalline inclusion bodies

•

en:lymphography shows hypoplasia of lymphatic vessels

•

en:low muscle mass

•

en:hypotonia, infantile, severe

•

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

•

en:lower limbs more affected than upper limbs

•

en:large hypertrophied fibers

•

en:isolated necrotic fibers

•

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

•

en:inclusion body myopathy

•

en:impaired heel-walking

•

en:upper limb involvement occurs later or not at all

•

en:usually no myopathic changes on biopsy

•

en:weakness of the anterior tibial muscle and toe extensors

•

en:muscle fibers may contain abnormal polysaccharide

•

en:pelvic muscle involvement occurs later

•

en:numerous vacuole-like areas

•

en:myosin storage myopathy (in some patients)

•

en:myopathy (in some patients)

•

en:muscle weakness (cvs+)

•

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

•

en:muscle biopsy shows ragged red fibers

•

en:poor muscle mass

•

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

•

en:muscle biopsy shows increased subsarcolemmal vacuolar glycogen accumulation

•

en:muscle biopsy shows glycogen storage

•

en:muscle biopsy shows decreased secondary clefts

•

en:muscle atrophy, especially quadriceps and forearm muscles

•

en:muscle atrophy, diffuse, severe

•

en:motor clumsiness

•

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

•

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

•

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

•

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

•

en:charcot-marie-tooth disease type 2q

•

en:abnormalities in myofibril organization

•

en:wasted lower leg muscles

•

en:unable to walk

•

en:type 2 fiber predominance

•

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

•

en:triceps aplasia

•

en:subsarcolemmal hyaline bodies in type 1 fibers only

•

en:prominent involvement of the quadriceps femoris muscles

•

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

•

en:small and incompletely fused muscle fibers seen on biopsy

•

en:slowly progressive limb-girdle myopathy

•

en:scapuloperoneal amyotrophy

•

en:rimmed vacuoles

•

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

•

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

•

en:mitochondrial proliferation

•

•

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

•

en:decreased activity of complexes ii+iii

•

en:degrading mitochondria

•

en:degenerating nerve terminals

•

en:decreased mitochondria

•

en:decreased cytochrome c oxidase activity

•

en:decreased complex i activity (rare)

•

en:decreased ant1 protein (103220) in muscle tissue

•

en:cytochrome c oxidase-negative fibers

•

en:emg shows decremental compound muscle action potential (cmap) in response to repetitive nerve stimulation

•

en:central cores seen on muscle biopsy

•

en:atrophy of the intrinsic foot and hand muscles

•

en:ankle reflex absent

•

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

•

en:abnormal sarcoplasmic reticulum elements

•

en:abnormal mitochondria in skeletal muscle biopsy

•

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

•

en:distal lower limb muscle weakness

•

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

•

en:exercise-induced weakness

•

en:increased variation in fiber size seen on muscle biopsy

•

en:fiber size variation

•

en:lower limbs more often affected

•

en:loss of subcutaneous adipose tissue in limbs

•

en:loss of antigravity strength

•

en:isolated mitochondrial complex iv deficiency seen on biopsy

•

en:inguinal hernia

•

en:independent walking may not be achieved

•

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

•

en:increased endo- and perimysial connective tissue

•

en:filamentous inclusions in muscle fibers

•

en:hyperactive deep tendon reflexes

•

en:global muscle weakness

•

en:generalized muscle weakness (less common)

•

en:generalized limb muscle atrophy

•

en:gait disturbance

•

en:inclusions form a lobulated structure seen on electron microscopy

•

en:imaging shows muscle atrophy and fatty replacement

•

en:inclusions are dnajb6-immunoreactive

•

en:increased connective tissue and fat in muscles

•

en:increased intermyofibrillar and subsarcolemmal glycogen

•

en:increased intramuscular fat

•

•

en:loss of subcutaneous fat, generalized

•

en:lack of integrin alpha-7 staining

•

en:limb lymphedema (in some patients)

•

en:loss of gluteal adipose tissue

•

en:loss of truncal subcutaneous adipose tissue

•

en:low maximum workload on exercise testing

•

en:lymphangiectasia

•

en:lymphedema (lower limb)

•

en:handgrip myotonia

•

en:lymphedema of lower limbs (in some patients)

•

en:distal lower limb amyotrophy

•

en:glycogen depletion in skeletal muscle

•

en:difficulty walking, running

•

en:macroglossia

•

en:decreased activity of respiratory complex i+iii

•

en:decreased density of calcium release units

•

en:decreased muscle mass (especially in lower limbs)

•

en:decreased numbers of type 2b fibers

•

en:decreased sarcolemmal immunostaining for ptrf

•

en:difficulty walking up stairs

•

en:fiber-type variability

•

en:distal limb muscular atrophy due to peripheral neuropathy

•

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

•

en:distal muscle atrophy due to peripheral neuropathy

•

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

•

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

•

en:emg shows neurogenic changes consistent with denervation

•

en:exercise-induced muscle stiffness

•

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

•

en:neurogenic changes

•

en:may have proximal muscle weakness later in the disease

•

en:sparing of small hand and finger muscles

•

en:prominent musculature

•

en:proximal limb muscle weakness initially

•

en:pyruvate oxidation defect

•

en:secondary myopathic features

•

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

•

en:skeletal muscle biopsy shows impaired respiratory oxidation

•

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

•

en:peroneal muscle atrophy

•

en:tubular aggregates in muscle fibers may occur

•

en:upper limb involvement may occur later

•

en:vacuolar myopathy

•

en:vacuolated muscle fibers show reduplication of the basement membrane

•

en:variable fiber size

•

en:winged scapula

•

en:z-line streaming see on electron microscopy

•

en:pharyngeal muscle weakness

•

en:normal or increased facial adipose tissue

•

en:minipolymyoclonus

•

en:muscle weakness, limb-girdle, mild

•

en:mri may show cervical spinal cord atrophy

•

•

en:muscle atrophy affecting the upper back and neck muscles

•

en:muscle atrophy in the limbs

•

en:muscle biopsy shows sarcoplasmic rods in myofibers

•

en:muscle wasting, severe, primarily in the legs

•

en:muscle weakness, lower limbs, during exercise

•

en:nemaline bodies

•

en:muscle weakness lower limb

•

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

•

en:myopathic and neurogenic changes seen on emg

•

en:myopathic changes seen on biopsy

•

•

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

•

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

•

en:bulbar weakness

◀

en:mitochondrial

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

• This page link : https://www.jeuxdemots.org/diko.php?gotermid=7119962 • caches: c1=8 c2=1003 c3=1

po

la

ti

le

as

ku

co

lo

to

ta

ta

xe

po

li

?!

!?

[Vider le cache]

A propos

Champs masqués

8.2 s