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Amyotrophy
Charcot-Marie-Tooth disease
Duchenne disease
Duchenne dystrophy
Duchenne muscular dystrophy
Duchenne type muscular dystrophy
Duchenne-Griesinger disease
Erb atrophy
Erb dystrophy
Facioscapulohumeral muscular atrophy
Facioscapulohumeral muscular dystrophy
Kennedy disease
Kennedy's disease
Landouzy-Dejerine dystrophy
Muscle atrophy
Muscle wasting
Muscular atrophy
Muscular idiopathic atrophy
Muscular neuritic atrophy
Neuritic atrophy
Peroneal muscular atrophy
Progressive neuromuscular atrophy
SBMA
Spinal and bulbar muscular atrophy
Spinobulbar muscular atrophy
X-linked spinal and bulbar muscular atrophy
Zimmerlin atrophy

Vertaling van "muscular neuritic atrophy " (Engels → Frans) :

muscular neuritic atrophy

atrophie musculaire névritique




muscular idiopathic atrophy

atrophie musculaire idiopathique


spinal and bulbar muscular atrophy | SBMA | Kennedy disease | X-linked spinal and bulbar muscular atrophy | spinobulbar muscular atrophy | Kennedy's disease

maladie de Kennedy | atrophie musculaire spinale et bulbaire | atrophie spinale bulbo-musculaire | amyotrophie spinobulbaire | SBMA


Duchenne muscular dystrophy [ Duchenne type muscular dystrophy | Duchenne dystrophy | Duchenne disease | Erb dystrophy | Duchenne-Griesinger disease | Zimmerlin atrophy | Erb atrophy ]

maladie de Duchenne de Boulogne


Charcot-Marie-Tooth disease | peroneal muscular atrophy | progressive neuromuscular atrophy

maladie de Charcot-Marie | syndrome de Charcot-Marie | atrophie de Charcot-Marie | atrophie péronière | amyotrophie de Charcot-Marie-Tooth


amyotrophy | muscle atrophy | muscular atrophy

amyotrophie | fonte musculaire | atrophie musculaire


muscle atrophy [ muscle wasting | muscular atrophy ]

amyotrophie [ atrophie musculaire | fonte musculaire ]


Landouzy-Dejerine dystrophy [ facioscapulohumeral muscular dystrophy | facioscapulohumeral muscular atrophy ]

myopathie facio-scapulo-humérale de Landouzy Déjerine [ myopathie facio-scapulo-humérale | myopathie de Landouzy-Déjerine ]


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

myopathie liée à l'X avec atrophie des muscles posturaux


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