Article
Neonatal-onset genetic epilepsies: Insights from a large multicentre cohort.
Seizure - 1 Jul 2026
Basarir Gunce, Gençpınar Pınar, Bozkaya Yılmaz Sema, Özyılmaz Berk, Olgaç Dündar Nihal, Türkdoğan Dilşad, Özcan Sermin, Polat Hamza, Karakayalı Burcu, Öztürk Gülten, Ünver Olcay, Cansu Ali, Yıldız Nihal, Kart Pınar Özkan, Aydın Kürşad, Topçu Yasemin, Özpınar Esra, Yılmaz Sanem, Kanmaz Seda, Per Hüseyin, Canpolat Mehmet, Gümüş Hakan, Güleç Ayten, Yıldırım Nalan, Eldeş Hacıfazlıoğlu Nilüfer, Uyur Emek, Teber Serap, Bektaş Ömer, Yıldırım Miraç, Değerliyurt Aydan, Gültutan Pembe, Okuyaz Çetin, Direk Meltem Çobanoğulları, Çağlar Ezgi, Ünay Bülent, Coşkun Ayşe Nur, Şimşek Erdem, Hız Kurul Semra, Aykol Duygu, Tosun Ayşe, Oktay Seçil, Polat Muzaffer, Ayca Senem, Atasever Aslı Kübra, Çarman Kürşat Bora, Yarar Coşkun, Yücel Şen Arife Derda, Aksu Uzunhan Tuğçe, Eser Metin, Dokurel Çetin İpek, Tekgül Hasan
Abstract excerpt
PURPOSE: Neonatal-onset genetic epilepsies are clinically heterogeneous and are increasingly diagnosed through genomic testing. We aimed to describe the phenotypes and neurodevelopmental outcomes of infants with neonatal-onset genetic epilepsy from eighteen tertiary centres and to explore subgroup differences across functional gene categories. METHODS: This retrospective multicentre study included 144 infants...
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