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CMT
Charcot-Marie-Tooth disease
Disease Charcot-Marie-Tooth
Déjerine-Sottas
HMSN
Hereditary motor and sensory neuropathy
PMA
Peripheral neuropathy
Peripheral sensory neuropathy
Peroneal muscular atrophy
Recessively inherited

Vertaling van "peripheral sensory neuropathy " (Engels → Nederlands) :

peripheral sensory neuropathy

neuropathie van de zintuigzenuwen in de extremiteiten


A very rare progressive and untreatable disease with manifestations of ataxia with sensory neuropathy. Prevalence is unknown, typically starts in middle-aged adults and presents with cerebellar ataxia, pyramidal signs, and peripheral sensory loss. Th

spinocerebellaire ataxie type 4


A rare form of axonal peripheral sensorimotor neuropathy with characteristics of classical Charcot-Marie-Tooth type 2 signs and symptoms (progressive weakness and atrophy of distal limb muscles, mild sensory deficits of position, vibration and pain/t

autosomaal dominante hereditaire motorische en sensorische neuropathie type 2 door 'kinesin family member 5A'-mutatie


A rare syndrome with the association of congenital hypertrichosis in the anterior cervical region, peripheral sensory and motor neuropathy. It has been described in three members of the same family and in one unrelated boy. Associated features in the

cervicale hypertrichose, perifere neuropathie


Charcot-Marie-Tooth disease | hereditary motor and sensory neuropathy | peroneal muscular atrophy | CMT [Abbr.] | HMSN [Abbr.] | PMA [Abbr.]

hereditaire motorische en sensorische neuropathie | ziekte van Charcot-Marie-Tooth | HMSN [Abbr.]


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

hereditaire motorische- en sensorische-neuropathie, type I-IV | infantiele hypertrofische-neuropathie | peroneale spieratrofie (axonaal type)(hypertrofisch type) | syndroom van Roussy-Lévy | ziekte van | Charcot-Marie-Tooth | ziekte van | Déjerine-Sottas


Morvan's disease Nelaton's syndrome Sensory neuropathy:dominantly inherited | recessively inherited

sensorische neuropathie | dominant erfelijk | sensorische neuropathie | recessief erfelijk | syndroom van Nelaton | ziekte van Morvan


Hereditary motor and sensory neuropathy

hereditaire motorische- en sensorische-neuropathie






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'peripheral sensory neuropathy' ->

Date index: 2021-03-26
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