Open AccessPatient with Dravet syndrome: A case report
Author(s) -
Yadav Rukesh,
Shah Sangam,
Bhandari Bibek,
Marasini Kundan,
Mandal Prince,
Murarka Hritik,
Pandey Anuj Kumar,
Sharma Paudel Basanta
Publication year - 2022
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.5840
Subject(s) - dravet syndrome , medicine , pediatrics , epilepsy , atrophy , encephalopathy , epilepsy syndromes , psychiatry
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.