A pediatric patient with Warsaw breakage syndrome presenting with epilepsy: a case report and literature review
BackgroundWarsaw breakage syndrome (WABS) is a rare disease caused by mutations in the DDX11 gene. It is characterized by severe growth restriction, microcephaly, and sensorineural hearing loss, and reports of coexisting epilepsy are even rarer. There are no studies on the focused synthesis of epile...
Kaydedildi:
| Asıl Yazarlar: | , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Frontiers Media S.A.
2026-03-01
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| Seri Bilgileri: | Frontiers in Neuroscience |
| Konular: | |
| Online Erişim: | https://www.frontiersin.org/articles/10.3389/fnins.2026.1751535/full |
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