Long-Term Seizure and Neurodevelopmental Outcomes of Three Children with Developmental Delay, Epilepsy, and Neonatal Diabetes (DEND) Syndrome after Early Initiation of Sulphonylurea

Developmental delay, epilepsy, and neonatal diabetes (DEND) syndrome, caused by de novo mutations in ABCC8/KCNJ11 genes encoding Adenosine Triphosphate (ATP)-sensitive potassium channels, is an unusual cause of infantile-onset developmental/epileptic encephalopathy. Here, we report the long-term sei...

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Autors principals:	Neena Baby, Kollencheri P Vinayan, Praveen Pavithran, Kshitij Bansal, Nisha Bhavani, Yatheesha B Lokeshappa, Arun G Roy
Format:	Artigo
Idioma:	Inglês
Publicat:	Wolters Kluwer Medknow Publications 2025-09-01
Col·lecció:	Annals of Indian Academy of Neurology
Matèries:	neonatal diabetes developmental delay seizure abcc8 mutation kcnj11 mutation sulfonylurea
Accés en línia:	https://journals.lww.com/10.4103/aian.aian_1097_24
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