Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies)

Dürr, Alexandra; Smadja, Didier; Cancel‐Tassin, Géraldine; Lézin, Agnès; Stévanin, Giovanni; Mikol, Jacqueline; Bellance, Rémy; Buisson, G; Chneiweiss, Hervé; Dellanavc, Janine; Agid, Yves; Brice, Alexis; Vernant, Jean‐Claude

doi:10.1093/brain/118.6.1573

Public

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies)

Published in Brain • Jan 1, 1995

Authors:

Alexandra Dürr

Didier Smadja

Géraldine Cancel‐Tassin

Abstract

Autosomal dominant cerebellar ataxia type I was diagnosed in three unrelated families from Martinique (French West Indies), and linkage to the locus for spinocerebellar ataxia 2 (SCA2) was established. Neuropathological findings in two patients were those of olivopontocerebellar atrophy without olig...

Subject

Ataxia

Age of onset

Olivopontocerebellar atrophy

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