Diko : en:muscle fiber atrophy, profound (rare)

en:muscle fiber atrophy, profound (rare)

Catégories

Nom

Informations lexicales

Langue:anglais

Liens externes

›

umls:C3281168

Associations d'idées

[F]

›

50+

en:wide variation in fiber size

•

en:normal muscle fiber (hcs)

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

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

•

en:decreased caveolin-3 expression on muscle biopsy

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

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en:electromyogram abnormal

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en:generalized amyotrophy

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en:increased muscle glycogen content

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en:muscle weakness, mainly proximal and axial

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en:myositis (in some patients)

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en:nemaline rod formation

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

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en:positive staining for atpase activity at ph of 4.3

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

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en:normal histopathology seen on muscle biopsy (in some patients)

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en:muscle weakness restricted to the upper limb

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en:muscle atrophy restricted to the upper limb

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

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en:internal nuclei

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en:head drop due to neck muscle weakness

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en:fiber size variation (in some patients)

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en:changes in sarcoplasmic reticulum and t-tubules

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en:axial muscle weakness

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en:atrophic calf muscles

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

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en:enlarged mitochondria

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en:hypotonia (patient b)

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en:internal nuclei (in some patients)

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en:lipohypoplasia, regional

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en:muscle biopsy shows sarcoplasmic pas-positive vacuoles

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en:muscle weakness and atrophy, upper and lower limbs

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en:proximal muscle weakness (120270.0002)

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en:cellulitis in lower limbs, recurrent

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en:distal lower limb amyotrophy

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en:exertional fatigue

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en:increased mitochondria with rare paracrystalline inclusions

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

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en:muscle pain with exercise (in older patients)

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en:potassium sensitivity has been reported

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en:ragged red fibers (in some patients)

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en:type 2 muscle fiber predominance

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en:congophilic amyloid material

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

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en:focal degeneration of junctional folds ('honeycombed' appearance) see on muscle biopsy

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en:humeroperoneal weakness and atrophy

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en:isolated mitochondrial complex iv deficiency seen on biopsy

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en:leg edema

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en:muscle weakness, upper and lower limbs

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en:ragged red fibers, mainly in type i fibers seen on skeletal muscle biopsy

▶

‹

50+

faiblesse de muscle

•

en:muscle weakness

•

en:paresis

•

faiblesse du muscle

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faiblesse musculaire

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parésie

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paralysie générale

•

parésie musculaire

•

omphalocèle

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hernie ombilicale congénitale

•

en:omphalocele

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hernie ombilicale

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exomphale

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omphalocèles

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exomphale congénitale

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en:umbilical hernia

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hernies ombilicales

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atrophie

•

en:atrophy

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oedème

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en:edema

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Oedème

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en:cytochrome-c oxidase deficiency

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déficit en cytochrome oxydase

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contraction clonique

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fasciculation d'un muscle squelettique

•

en:muscle twitch

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secousse musculaire

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en:twitching

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en:fasciculation

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en:muscular fasciculation

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déficit en cytochrome-c oxydase

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en:general paresis

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œdème

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en:Umbilical hernia

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en:hypotonia

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lipome

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hypotonie

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en:lipoma

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en:dysphagia

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Autophagosome

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dysphagie

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autophagosome

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parésié

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dysphagia

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en:broad-based gait

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élargissement du polygone de sustentation

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empâtement de la nuque et du cou

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en:buffalo hump

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en:wide-based gait

▶

Génériques

[F] [H]

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en:muscle

• Mathieu Lafourcade • LIRMM (données libres en Creative Commons) •

• This page link : https://www.jeuxdemots.org/diko.php?gotermid=7118625 • caches: c1=44 c2=279 c3=2088

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