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一名患有自闭症特征、癫痫、发育迟缓、特应性皮炎和免疫异常的男孩,其22号染色体长臂13.2区至末端存在一个7.9兆碱基的新发缺失。

A de novo 7.9 Mb deletion in 22q13.2→qter in a boy with autistic features, epilepsy, developmental delay, atopic dermatitis and abnormal immunological findings.

作者信息

Chen Chih-Ping, Lin Shuan-Pei, Chern Schu-Rern, Tsai Fuu-Jen, Wu Pei-Chen, Lee Chen-Chi, Chen Yu-Ting, Chen Wen-Ling, Wang Wayseen

出版信息

Eur J Med Genet. 2010 Sep-Oct;53(5):329-32. doi: 10.1016/j.ejmg.2010.06.004. Epub 2010 Jun 9.

Abstract

We report a 5-year-old boy with mental retardation, autistic features, epilepsy, developmental delay, atopic dermatitis and abnormal immunological findings, carrying a 7.9 Mb de novo deletion of chromosome 22q13.2→qter. This region contains the SHANK3, NCAPH2 and CYP2D6 genes which are associated with T-cell immune response. The present case provides evidence that 22q13 deletion syndrome may be associated with immune system dysfunction in addition to neuropsychiatric disorders.

摘要

我们报告了一名5岁男孩,患有智力障碍、自闭症特征、癫痫、发育迟缓、特应性皮炎以及异常免疫检查结果,其22号染色体发生了7.9 Mb的从头缺失,缺失区域为22q13.2→qter。该区域包含与T细胞免疫反应相关的SHANK3、NCAPH2和CYP2D6基因。本病例提供了证据,表明22q13缺失综合征除了与神经精神疾病有关外,还可能与免疫系统功能障碍有关。

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