Spinocerebellar ataxia with epilepsy

MONDO:0016809

A rare, mitochondrial DNA maintenance syndrome characterized by cerebellar ataxia, sensory peripheral neuropathy, myoclonus, epilepsy, progressive cognitive impairment, late-onset ptosis and external ophthalmoplegia. Liver failure may also occur, most often in association with the use of antiepileptic drug sodium valproate.

Also known as: MSCAE, SCAE, mitochondrial spinocerebellar ataxia with epilepsy

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