Vertaling van "Charcot-Marie-Tooth disease " (Engels → Frans) :

Charcot-Marie-Tooth disease, type 4B2 (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso
maladie de Charcot-Marie-Tooth type 4B2

Charcot-Marie-Tooth disease [ peroneal muscular atrophy ]
maladie de Charcot-Marie-Tooth

Charcot-Marie-Tooth disease | CMT [Abbr.]
maladie de Charcot-Marie-Tooth

Charcot-Marie-Tooth disease | hereditary motor and sensory neuropathy | peroneal muscular atrophy | CMT [Abbr.] | HMSN [Abbr.] | PMA [Abbr.]
amyotrophie péronière de Charcot-Marie-Tooth | CMT | maladie de Charcot-Marie-Tooth | neuropathie héréditaire de Charcot-Marie-Tooth

Charcot-Marie-Tooth Disease Peroneal Muscular Atrophy International Association, Inc.
Charcot-Marie-Tooth Disease Peroneal Muscular Atrophy International Association, Inc.

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

peroneal muscular atrophy | Charcot Marie-Tooth disease
amyotrophie péronière | syndrome de Charcot-Marie-Tooth-Hoffmann

Autosomal dominant Charcot-Marie-Tooth disease type 2K
maladie de Charcot-Marie-Tooth autosomique dominante type 2K

Autosomal dominant Charcot-Marie-Tooth disease type 2N
maladie de Charcot-Marie-Tooth autosomique dominante type 2N

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
Amyotrophie péronière (type axonal) (type hypertrophique) Maladie de:Charcot-Marie-Tooth | Déjerine-Sottas | Neuropathie:héréditaire motrice et sensorielle, types I-IV | hypertrophique de l'enfant | Syndrome de Roussy-Lévy