Leigh’s Syndrome with Two Mitochondrial Defects

J Gordon Millichap

doi:10.15844/pedneurbriefs-6-2-5

Leigh’s Syndrome with Two Mitochondrial Defects

Pediatric Neurology Briefs

Volume 6 (1992): Issue 2

By: J Gordon Millichap

Open Access

|Feb 1992

Abstract

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

References

Reichmann H Scheel H Bier B Ketelsen UP Zabransky S Cytochrome c oxidase deficiency and long-chain acyl coenzyme A dehydrogenase deficiency with Leigh’s subacute necrotizing encephalomyelopathy Ann Neurol 1992 Jan 31 1 107 109 10.1002/ana.410310120 1311909
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-6-2-5 | Journal eISSN: 2166-6482

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Language: English

Page range: 11 - 12

Published on: Feb 1, 1992

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Leigh’s Syndrome,

Mitochondrial Enzyme,

Dehydrogenase Deficiency

© 1992 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 6 (1992): Issue 2