Spinocerebellar ataxia 27: A rare genetic disorder (chromosome FGF14; 13q34 defect) characterized by tremors, dyskinesia and psychiatric episodes. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types. More detailed information about the symptoms, causes, and treatments of Spinocerebellar ataxia 27 is available below.
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Prognosis for Spinocerebellar ataxia 27: normal life expectancy with major walking problems by 7th or 8th decade
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