| Literature DB >> 6417559 |
P L Holliday, A R Climie, J Gilroy, M Z Mahmud.
Abstract
We describe three patients with mitochondrial myopathy, dementia, loss of vision and hearing, seizure disorder with myoclonus, intermittent headaches of a vascular type, visual hallucinations, cerebellar dysfunction, and lactic acidosis. Muscle biopsies in all patients and liver biopsy in one revealed abnormal mitochondria. The disorder may be due to a deficiency of mitochondrial NADH-CoQ dehydrogenase.Entities:
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Year: 1983 PMID: 6417559 DOI: 10.1212/wnl.33.12.1619
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910