Mitochondrial Myopathy and Congenital Cataract

J Gordon Millichap

doi:10.15844/pedneurbriefs-7-5-7

Mitochondrial Myopathy and Congenital Cataract

Pediatric Neurology Briefs

Volume 7 (1993): Issue 5

By: J Gordon Millichap

Open Access

|May 1993

Abstract

The autosomal recessive syndrome characterized by mitochondrial myopathy of cardiac and skeletal muscle, congenital cataract and lactic acidosis is described in two forms following a retrospective study of 16 patients at the University of Nijmegen, The Netherlands.

References

van Ekeren GJ Stadhouders AM Smeitink JA Sengers RC A retrospective study of patients with the hereditary syndrome of congenital cataract, mitochondrial myopathy of heart and skeletal muscle and lactic acidosis Eur J Pediatr 1993 Mar 152 3 255 9 8444256 10.1007/BF01956157
Open DOI Search in Google Scholar Back to article

Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-7-5-7 | Journal eISSN: 2166-6482

Journal RSS Feed

Language: English

Page range: 36 - 37

Published on: May 1, 1993

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Recessive Syndrome,

Cardiomyopathy,

Subvalvular Aortic

© 1993 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 7 (1993): Issue 5