Vertaling van "Peroneal muscular atrophy " (Engels → Nederlands) :

Charcot-Marie-Tooth disease | hereditary motor and sensory neuropathy | peroneal muscular atrophy | CMT [Abbr.] | HMSN [Abbr.] | PMA [Abbr.]
hereditaire motorische en sensorische neuropathie | ziekte van Charcot-Marie-Tooth | HMSN [Abbr.]

Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome
hereditaire motorische- en sensorische-neuropathie, type I-IV | infantiele hypertrofische-neuropathie | peroneale spieratrofie (axonaal type)(hypertrofisch type) | syndroom van Roussy-Lévy | ziekte van | Charcot-Marie-Tooth | ziekte van | Déjerine-Sottas

Aran-Duchenne disease | Cruveilhier disease | PMA | progressive muscular atrophy | progressive spinal muscular atrophy | spinal muscular atrophy | spinal progressive muscular atrophy | SMA [Abbr.] | SPMA [Abbr.]
spieratrofie van Aran-Duchenne | ziekte van Duchenne-Aran

infantile spinal muscular atrophy | progressive muscular atrophy of infancy | severe infantile spinal muscular atrophy | spinal muscular atrophy type I | Werdnig-Hoffman disease | SMA I [Abbr.]
infantiele spinale spieratrofie | Spinale musculaire atrofie type I | ziekte van Werdnig-Hoffmann | SMA type I [Abbr.]

A rare progressive muscular dystrophy characterized by an adult-onset scapulo-axio-peroneal myopathy. Clinical presentation includes shoulder girdle atrophy, scapular winging, axial muscular atrophy of postural muscles combined with a generalized hyp
X-gebonden myopathie met posturale spieratrofie

Spinal muscular atrophy and related syndromes
spinale spieratrofie en verwante syndromen

Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
infantiele spinale-spieratrofie, type I [Werdnig-Hoffman]

Autosomal dominant benign distal spinal muscular atrophy
autosomaal dominante congenitale goedaardige spinale spieratrofie

Autosomal recessive distal spinal muscular atrophy 1
autosomaal recessieve distale spinale musculaire atrofie type 1