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Patient with Dravet syndrome: A case report |
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| Authors: | Rukesh Yadav Sangam Shah Bibek Bhandari Kundan Marasini Prince Mandal Hritik Murarka Anuj Kumar Pandey Basanta Sharma Paudel |
| Affiliation: | 1. Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Maharajgunj Nepal ; 2. Department of Internal Medicine, Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Maharajgunj Nepal ; 3. Department of Radiology, Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Maharajgunj Nepal ; 4. Tribhuvan University Teaching Hospital, Maharajgunj Nepal |
| 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. |
| Keywords: | dravet SCN1A syndrome |