Article
Spinocerebellar ataxia type 14.
Handbook of clinical neurology - 1 Jan 2012
Chen Dong-Hui, Raskind Wendy H, Bird Thomas D
Abstract excerpt
SCA14 is an autosomal dominant hereditary cerebellar ataxia that usually has an onset in early to mid adult life, with slow progression and normal lifespan. Although generally an uncomplicated cerebellar ataxia with gait imbalance, dysarthria, and nystagmus, there is occasionally sensory loss, hyperactive tendon reflexes, cognitive decline, or myoclonus. Brain MRI shows cerebellar atrophy. A single autopsy has...
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