A rare genetic neurological disorder characterized by late childhood onset of slowly progressive cerebellar ataxia. Initial manifestations include weakness and atrophy of distal limb muscles, areflexia and loss of pain, vibration and touch sensations

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

syndrome d'ataxie spinocérébelleuse-neuropathie axonale type 1

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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

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neuropathie sensitivo-motrice héréditaire type Okinawa

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An extremely rare mitochondrial respiratory chain disease resulting in a neurodegenerative disorder with characteristics of psychomotor delay, hypotonia, areflexia, muscle weakness and wasting in the two patients reported to date. Combined oxidative

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encéphalomyopathie mitochondriale sévère liée à l'X

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D'autres ont cherché : abdominal wall areflexia absent reflexes absent tendon reflexes areflexia corneal areflexia semilateral areflexia of abdominal skin tendon areflexia Areflexia

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'Areflexia' ->

Date index: 2022-07-28