Mitochondrial Myopathy and Congenital Cataract
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.
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
1993-05-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/2958 |