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Severe myoclonic epilepsy and mitochondrial cytopathy

✍ Scribed by M. Castro-Gago; J. Eirís-Puñal; J. M. Martinón Sánchez; A. Rodríguez-Nuñez; J. L. Herranz Fernández

Publisher
Springer
Year
1997
Tongue
English
Weight
35 KB
Volume
13
Category
Article
ISSN
0256-7040

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## Abstract We report on 2 adult patients presenting with choreic movements as the main clinical feature of mitochondrial cytopathy. One patient exhibited a sensory neuronopathy and ophthalmoplegia. The other had ptosis, a proximal myopathy, and a sensory neuropathy. The diagnosis of mitochondrial