Coppola Antonietta, Morrogh Deborah, Farrell Fiona, Balestrini Simona, Hernandez-Hernandez Laura, Krithika S, Sander Josemir W, Waters Jonathan J, Sisodiya Sanjay M
Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, London, UK.
Chalfont Centre for Epilepsy, Chalfont St Peter, UK.
Mol Syndromol. 2017 Dec;9(1):38-44. doi: 10.1159/000479949. Epub 2017 Sep 15.
Chromosomal abnormalities are often identified in people with neurodevelopmental disorders including intellectual disability, autism, and epilepsy. Ring chromosomes, which usually involve gene copy number loss, are formed by fusion of subtelomeric or telomeric chromosomal regions. Some ring chromosomes, including ring 14, 17, and 20, are strongly associated with seizure disorders. We report an individual with a ring chromosome 17, r(17)(p13.3q25.3), with a terminal 17q25.3 deletion and no short arm copy number loss, and with a phenotype characterized by intellectual disability and drug-resistant epilepsy, including a propensity for nonconvulsive status epilepticus.
染色体异常在患有神经发育障碍(包括智力残疾、自闭症和癫痫)的人群中经常被发现。环状染色体通常涉及基因拷贝数丢失,由亚端粒或端粒染色体区域融合形成。一些环状染色体,包括14号、17号和20号环状染色体,与癫痫发作障碍密切相关。我们报告了一名患有17号环状染色体r(17)(p13.3q25.3)的个体,该个体存在17q25.3末端缺失且无短臂拷贝数丢失,其表型特征为智力残疾和耐药性癫痫,包括非惊厥性癫痫持续状态的倾向。