Department of Neonatology, CHU de Saint-Etienne, Saint Etienne, France.
Epileptic Disord. 2011 Sep;13(3):331-5. doi: 10.1684/epd.2011.0446.
Angelman syndrome is a rare genetic disorder scarcely diagnosed before the age of two years. We report the case of an eight-month-old female presenting with severe hypotonia, myoclonus, suspected spasms and an electroencephalogram with hypsarrhythmic-like features. She was initially treated with vigabatrin which resulted in worsening of myoclonic jerks. Fluorometric in situ hybridization revealed a chromosomal deletion at region 15q11-13. We discuss the case and differential diagnosis with other conditions including West syndrome. [Published with video sequences].
安琪曼综合征是一种罕见的遗传疾病,在两岁之前很少被诊断出来。我们报告了一例 8 个月大的女性病例,表现为严重的低张力、肌阵挛、疑似痉挛和脑电图呈现出类高度失律特征。她最初接受了氨己烯酸治疗,导致肌阵挛性抽搐恶化。荧光原位杂交显示 15q11-13 区域的染色体缺失。我们讨论了该病例,并与包括 West 综合征在内的其他疾病进行了鉴别诊断。[附有视频序列]。