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Déjerine-Sottas
Hypertrophique de l'enfant
Neuropathie héréditaire motrice et sensorielle
Neuropathie motrice distale héréditaire type 1
Neuropathie motrice distale héréditaire type 7
Neuropathie motrice distale héréditaire type Jerash
Neuropathie sensitivo-motrice héréditaire type 5
Neuropathie sensitivo-motrice héréditaire type Okinawa
Syndrome de Roussy-Lévy

Translation of "motrice distale héréditaire " (French → English) :

neuropathie motrice distale héréditaire de l'adulte jeune

Autosomal recessive distal spinal muscular atrophy type 5
SNOMEDCT-BE (disorder) / 771475006
SNOMEDCT-BE (disorder) / 771475006


neuropathie motrice distale héréditaire type 7

Distal hereditary motor neuropathy type 7
SNOMEDCT-BE (disorder) / 771081007
SNOMEDCT-BE (disorder) / 771081007


neuropathie motrice distale héréditaire type 1

Autosomal dominant distal juvenile spinal muscular atrophy type 1
SNOMEDCT-BE (disorder) / 770630005
SNOMEDCT-BE (disorder) / 770630005


neuropathie motrice distale héréditaire type Jerash

Autosomal recessive distal spinal muscular atrophy type 2
SNOMEDCT-BE (disorder) / 763533003
SNOMEDCT-BE (disorder) / 763533003


neuropathie sensitivo-motrice axonale héréditaire avec acrodystrophie

A rare axonal hereditary motor and sensory neuropathy with characteristics of progressive axonal neuropathy with limb weakness and severe distal sensory loss in all limbs and acrodystrophic changes leading to painless non-healing ulcers, osteomyeliti
SNOMEDCT-BE (disorder) / 771144005
SNOMEDCT-BE (disorder) / 771144005


paralysie périodique avec neuropathie motrice distale tardive

A rare genetic neuromuscular disease with characteristics of acute episodic muscle weakness in upper and lower extremities (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy.
SNOMEDCT-BE (disorder) / 774154008
SNOMEDCT-BE (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy. / 774154008


Neuropathie héréditaire motrice et sensorielle

Hereditary motor and sensory neuropathy
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0


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

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
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0


neuropathie sensitivo-motrice héréditaire type 5

Charcot-Marie-Tooth disease, pyramidal features syndrome
SNOMEDCT-BE (disorder) / 771143004
SNOMEDCT-BE (disorder) / 771143004


neuropathie sensitivo-motrice héréditaire type Okinawa

An autosomal dominant form of hereditary motor and sensory neuropathy with dominant proximal involvement. Manifestations include adult-onset proximal neurogenic atrophy, sensory involvement, painful muscle cramps, fasciculations, areflexia, and high
SNOMEDCT-BE (disorder) / 715665006
SNOMEDCT-BE (disorder) / 715665006




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motrice distale héréditaire

Date index:2022-03-25 -

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