患有德雷维特综合征的患者：一例病例报告。
Patient with Dravet syndrome: A case report.
作者信息
Yadav Rukesh, Shah Sangam, Bhandari Bibek, Marasini Kundan, Mandal Prince, Murarka Hritik, Pandey Anuj Kumar, Sharma Paudel Basanta
机构信息
Maharajgunj Medical Campus Institute of Medicine Tribhuvan University Maharajgunj Nepal.
Department of Internal Medicine Maharajgunj Medical Campus Institute of Medicine Tribhuvan University Maharajgunj Nepal.
出版信息
Clin Case Rep. 2022 May 5;10(5):e05840. doi: 10.1002/ccr3.5840. eCollection 2022 May.
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.
德雷维特综合征是一种罕见的遗传性癫痫综合征和癫痫性脑病。患者最初发育正常，在癫痫发作后开始出现发育停滞或倒退。我们报告了一例两岁儿童被诊断为德雷维特综合征，伴有中度脑萎缩和脑室扩张，这是罕见的磁共振成像（MRI）表现。
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