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KMID : 0359719950130020396
Journal of the Korean Neurological Association
1995 Volume.13 No. 2 p.396 ~ p.399
A Case of Hereditary Spastic Ataxia
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Abstract
Hereditary spastic ataxia is a familial neurological disorder which exhibit the features of a progressive combined pyramidal tract and cerebellar deficiency. The main features are progressive gait disturbance. incoordination. Nystagmus, visual
impairment, hyperreflexia, extensor plantar response, peripheral neuropathy, and pes cavus.
A 27-year-old male patient with spastic ataxic gait was evaluated. He showed characteristic features of hereditary spastic ataxia. There were another twelve affected members in four generations of his family which may be inherited by autosomal
dominant
pattern. One of them is reported with review of the literature on familial spastic ataxia.
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