Leighs Syndrome with Two Mitochondrial Defects

Abstract

A female infant with a biochemical defect of the respiratory chain and of -oxidation and neuropathological changes typical for Leighs disease is reported from the Department of Neurology, University of Wrzburg, Departments of Pediatrics and Pathology, University of Homburg, and Department of Pediatrics, University of Freiburg, Germany.

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