Mitochondrial Myopathy and Hypotonia

J Gordon Millichap

doi:10.15844/pedneurbriefs-6-5-8

Mitochondrial Myopathy and Hypotonia

Pediatric Neurology Briefs

Volume 6 (1992): Issue 5

By: J Gordon Millichap

Open Access

|May 1992

Abstract

Three children with hypotonia, cardiac impairment, and defects of the mitochondrial respiratory chain complexes, but no ragged red fibers, are reported from the Hopital de la Timone, Chemin de l’Armee, d’Afrique, Marseille, France.

References

Figarella-Branger D Pellissier JF Scheiner C Wernert F Desnuelle C Defects of the mitochondrial respiratory chain complexes in three pediatric cases with hypotonia and cardiac involvement J Neurol Sci 1992 Mar 108 1 105 113 10.1016/0022-510X(92)90195-Q 1320661
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Bertini E Neurology 1992 April 42 Suppl 3 267 10.1212/WNL.42.1.267
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-6-5-8 | Journal eISSN: 2166-6482

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Language: English

Page range: 38 - 39

Published on: May 1, 1992

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Mitochondrial Myopathy,

Neonatal Hypotonia,

Lactate/Pyruvate

© 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 5