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  1. Tan CT
    Med J Malaysia, 1980 Dec;35(2):134-8.
    PMID: 7266406
    An Indian family with four members having hereditary ataxia was presented. The inheritance was most likely autosomal dominant. The onset was at adult life. The main disability was cerebellar ataxia with pyramidal tract sign found at physical examination. Electroencephalography and nerve conduction study were abnormal in two cases where they were done. The clinical feature correspond to an intermediate form of hereditary ataxia.
    Matched MeSH terms: Cerebellar Ataxia/classification
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