A rare hereditary ataxia with characteristics of delayed early motor development, severe neonatal hypotonia, non-progressive ataxia and slow eye movements, presenting normal cognitive abilities and absence of pyramidal signs. Frequently patients also

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syndrome de neurodégénérescence progressive de l'enfant-cécité-ataxie-spasticité

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A genetic neurodegenerative disease with normal early development followed by childhood onset optic atrophy with progressive vision loss and eventually blindness, followed by progressive neurological decline that typically includes cerebellar ataxia,

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Ataxie congénitale non progressive

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Congenital nonprogressive ataxia

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Date index: 2023-09-18