Sacquegna T, Montagna P, Moggio M, De Carolis P, Agati R, Bresolin N
Istituto di Clinica Neurologica, Università di Bologna.
Ital J Neurol Sci. 1989 Feb;10(1):73-5. doi: 10.1007/BF02333875.
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.