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6q22.33 微缺失与一家系的智力障碍、多种主要畸形和行为异常相关。

6q22.33 microdeletion in a family with intellectual disability, variable major anomalies, and behavioral abnormalities.

机构信息

Institut f, ü, r Klinische Genetik, Medizinische Fakult, ä, t Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.

Klinik und Poliklinik für Kinder-und Jugendmedizin, Universitätsklinikum Carl Gustav Carus, Dresden, Germany.

出版信息

Am J Med Genet A. 2015 Nov;167A(11):2800-7. doi: 10.1002/ajmg.a.37266. Epub 2015 Sep 3.

Abstract

Interstitial deletions on the long arm of chromosome six have been described for several regions including 6q16, 6q22.1, and 6q21q22.1, and with variable phenotypes such as intellectual disability/developmental delay, growth retardation, major and minor facial anomalies. However, an isolated microdeletion of the sub-band 6q22.33 has not been reported so far and thus, no information about the specific phenotype associated with such a copy number variant is available. Here, we define the clinical picture of an isolated 6q22.33 microdeletion based on the phenotype of six members of one family with loss of approximately 1 Mb in this region. Main clinical features include mild intellectual disability and behavioral abnormalities as well as microcephaly, heart defect, and cleft lip and palate.

摘要

已经描述了染色体 6 长臂上的几个区域的间质缺失,包括 6q16、6q22.1 和 6q21q22.1,并且具有不同的表型,如智力残疾/发育迟缓、生长迟缓、主要和次要面部异常。然而,迄今尚未报道 6q22.33 亚带的孤立微缺失,因此,对于与这种拷贝数变异相关的特定表型尚无信息。在这里,我们根据一个家族的六个成员在该区域缺失约 1 Mb 的表型来定义孤立的 6q22.33 微缺失的临床特征。主要临床特征包括轻度智力残疾和行为异常,以及小头畸形、心脏缺陷和唇裂腭裂。

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