SCA with ophthalmoparesis and hyperreflexia (medical condition)
A rare genetic disorder (chromosome 18p11 defect) characterized by eye muscle paralysis (ophthalmoplegia) and increased reflexes. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types. See also Spinocerebellar ataxia 28
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