Rare variants of mitochondrial DNA in a child with encephalomyopathy
The paper considers a clinical case of a child with suspected mitochondrial encephalomyopathy: cyclic vomiting, evident fatigue, muscle weakness, headache, and difficulties in learning school material. The similar symptoms are noted in an older sibling; the mother suffers from type 1 diabetes mellit...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
Ltd. “The National Academy of Pediatric Science and Innovation”
2016-11-01
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| Series: | Rossijskij Vestnik Perinatologii i Pediatrii |
| Subjects: | |
| Online Access: | https://www.ped-perinatology.ru/jour/article/view/378 |