Title : Ophthalmologic features of the common spinocerebellar ataxias

Abstract

Purpose of review: The spinocerebellar ataxias are a phenotypically and genetically diverse group of autosomal dominant disorders that cause pathological degeneration in the cerebellum, brainstem, and retina, resulting in a wide variety of ophthalmologic signs and symptoms. Recent findings: The genetic discrimination of the spinocerebellar ataxias has… (More)

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Cite this paper

@inproceedings{Pula2012TitleO, title={Title : Ophthalmologic features of the common spinocerebellar ataxias}, author={John H. Pula and Christopher M. Gomez}, year={2012} }