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Neuropathie sensitivo-motrice héréditaire type 5
Neuropathie sensitivo-motrice héréditaire type Okinawa
Polyneuropathie sensitivo-motrice

Translation of "polyneuropathie sensitivo-motrice " (French → English) :

polyneuropathie sensitivo-motrice

sensorimotor polyneuropathy
IATE - Health
IATE - Health


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


neuropathie sensitivo-motrice héréditaire type 5

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


syndrome de microcephalie-neuropathie sensitivo-motrice axonale complexe

An extremely rare subtype of hereditary motor and sensory neuropathy with characteristics of severe, rapidly progressing, distal, symmetric polyneuropathy and microcephaly (which can be evident in utero) with intact cognition. Clinically it presents
SNOMEDCT-BE (disorder) / 763798008
SNOMEDCT-BE (which can be evident in utero) with intact cognition. Clinically it presents / 763798008




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polyneuropathie sensitivo-motrice

Date index:2022-06-15 -

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