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Autosomal dominant Charcot-Marie-Tooth disease type 2K
Autosomal dominant Charcot-Marie-Tooth disease type 2N
CMT
Charcot Marie-Tooth disease
Charcot-Marie-Tooth disease
Disease Charcot-Marie-Tooth
Déjerine-Sottas
HMSN
Hereditary motor and sensory neuropathy
PMA
Peroneal muscular atrophy
Progressive neuromuscular atrophy

Traduction de «charcot-marie-tooth disease type » (Anglais → Français) :

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.


peroneal muscular atrophy | Charcot Marie-Tooth disease

amyotrophie péronière | syndrome de Charcot-Marie-Tooth-Hoffmann


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


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




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'charcot-marie-tooth disease type' ->

Date index: 2022-02-22
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