Patient with Dravet syndrome: A case report

oleh: Rukesh Yadav, Sangam Shah, Bibek Bhandari, Kundan Marasini, Prince Mandal, Hritik Murarka, Anuj Kumar Pandey, Basanta Sharma Paudel

Format: Article
Diterbitkan: Wiley 2022-05-01

Deskripsi

Abstract Dravet syndrome is rare genetic epilepsy syndrome and epileptic encephalopathy. The patient initially has normal developmental profile with plateau or regression that begins after seizure onset. We report a case of two‐year‐old child diagnosed as dravet syndrome with moderate cerebral atrophy and ventricular dilatation as rare MRI finding.