Difficulties of diagnostics of epilepsy due to molybdenum cofactor deficiency: a case report
The article presents a clinical study of an infant with rare inherited metabolism disorder – molybdenum cofactor deficiency, for the first time in Russian literature. The onset of disorder – in early neonatal period with a suppression syndrome and myoclonic seizures combined with a burstsuppression...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
ABV-press
2019-07-01
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| Series: | Russkij Žurnal Detskoj Nevrologii |
| Subjects: | |
| Online Access: | https://rjdn.abvpress.ru/jour/article/view/295 |