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Author

H. Aygün

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Review Open access Aug 2026

Epilepsy with eyelid myoclonia beyond the classical phenotype: Longitudinal electroclinical observations in a pediatric cohort.

OBJECTIVE Epilepsy with eyelid myoclonia is a childhood-onset generalized epilepsy syndrome with variable recognition of eyelid myoclonia, eye-closure sensitivity, and photosensitivity during follow-up. We aimed to characterize longitudinal clinical and electroencephalographic features in pediatric epilepsy with eyelid...

H. Aygün, Alper Taşkın, Özlem Yayıcı Köken et al. · 0 citations
Case report Open access Sep 2026

Pediatric Familial Cerebral Cavernous Malformation Associated With a Novel KRIT1 Initiation‐Region Frameshift Variant

Familial cerebral cavernous malformation is an autosomal dominant vascular disorder with age‐dependent penetrance and marked intrafamilial variability and genotype–phenotype correlations remain limited.

Özlem Yayıcı Köken, M. S. Yanartaş, H. Aygün et al. · 0 citations

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