Vertaling van "charcot-marie symptom " (Engels → Frans) :

Charcot-Marie symptom | Marie sign
signe de Charcot-Marie

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

A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 60 m/s). It presents with moderately severe, slowly progressive usual clinical features of Charcot-Marie-Too
maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante C

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

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

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

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

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

Autosomal recessive demyelinating Charcot-Marie-Tooth
maladie de Charcot-Marie-Tooth type 4