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Article
February 1962

Hereditary Ataxia of Rabbits: Histopathological Alterations

Author Affiliations

ST. LOUIS
From the Departments of Anatomy and Pathology, and Divisions of Neurology and Neurosurgery, Washington University School of Medicine, and the Jackson Memorial Laboratory, Bar Harbor, Me.

Arch Neurol. 1962;6(2):123-137. doi:10.1001/archneur.1962.00450200037004
Abstract

There is no disease of animals directly comparable with human cerebellar ataxia, although conditions variously designated as agenesis, hypoplasia, and atrophy are described. Dow and Moruzzi6 have reviewed this topic. A condition in the cat called olivopontocerebellar atrophy was reported by Schut17 as one of a number of recorded instances of hypoplasia in this species. Earlier, that topic had been reviewed by Brouwer,3 who noted the association of cerebellar hypoplasia with atrophy of the inferior olives and of the pontine nuclei. Brouwer and Biermond4 designated this condition, too, as olivopontocerebellar atrophy. In relation to the present study, it is important that Brouwer3 described the deep cerebellar nuclei as showing a usual cell content. It is also relevant that in the ataxias of man and of cat the tissue studied represents an end stage of the pathological process. In the study reported herein, clinical manifestations become

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