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Ital J Neurol Sci ; 10(1): 73-5, 1989 Feb.
Article in English | MEDLINE | ID: mdl-2925347

ABSTRACT

Mitochondrial encephalomyopathies may display clinical features similar to Ramsay-Hunt syndrome (RHS). We studied muscles mitochondrial function in 2 patients with RHS. Histochemical and ultrastructural studies of muscle biopsies and biochemical analysis of muscle mitochondrial enzymes were normal. There is no evidence for a disturbance of muscle mitochondrial function in RHS.


Subject(s)
Cerebellar Ataxia/enzymology , Mitochondria, Muscle/enzymology , Myoclonic Cerebellar Dyssynergia/enzymology , Adult , Humans , Male , Mitochondria, Muscle/pathology , Myoclonic Cerebellar Dyssynergia/pathology
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