Epilepsy in biotinidase deficiency
The specific features of epilepsy are analyzed in three siblings with biotinidase deficiency. The first sibling aged 10 months died in status epilepticus. The second baby was diagnosed with the disease at the age of 5 months. In the third sibling, pathogenetic treatment was started at birth. Emphasi...
| Main Authors: | , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
Ltd. “The National Academy of Pediatric Science and Innovation”
2016-03-01
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| Series: | Rossijskij Vestnik Perinatologii i Pediatrii |
| Subjects: | |
| Online Access: | https://www.ped-perinatology.ru/jour/article/view/238 |