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Dandy-Walker 畸形患者与 GJB2 基因(编码连接蛋白 26 的 p.Asp50Asn 突变)杂合突变相关的 KID 综合征。

Dandy-Walker malformation in patients with KID syndrome associated with a heterozygote mutation (p.Asp50Asn) in the GJB2 gene encoding connexin 26.

机构信息

Department of Otolaryngology, Unfallkrankenhaus Berlin, Charité Medical School, Berlin, Germany.

出版信息

Clin Genet. 2009 Oct;76(4):404-8. doi: 10.1111/j.1399-0004.2009.01211.x.

Abstract

The Keratitis-Ichthyosis-Deafness syndrome (KIDS) is an autosomal dominant ectodermal dysplasia characterized by ocular, skin, and ear anomalies, including keratitis, palmoplantar keratoderma, and congenital hearing loss. Most cases are due to mutations in the GJB2 gene encoding connexin 26. The Dandy-Walker malformation (DWM) is a developmental anomaly of the midline of the cerebellum with complete or partial agenesis of the vermis and cystic dilatation of the fourth ventricle. The association of KID syndrome with DWM has been reported a few times, but thought to be coincidental. We report 4 additional patients with KIDS and DWM, supporting the possibility that this is an association and not a coincidental finding. This also suggests that the GJB2 gene may have a role in other cases with DWM of, as yet, unknown etiology.

摘要

Keratitis-ichthyosis-deafness 综合征(KIDS)是一种常染色体显性遗传性外胚层发育不良,其特征为眼部、皮肤和耳部异常,包括角膜炎、掌跖角化病和先天性听力损失。大多数病例是由于编码连接蛋白 26 的 GJB2 基因突变所致。Dandy-Walker 畸形(DWM)是小脑中线的发育异常,表现为蚓部完全或部分缺失以及第四脑室囊性扩张。已有报道 KID 综合征与 DWM 相关数次,但认为这是偶然的。我们报告了另外 4 例 KIDS 和 DWM 患者,支持这是一种关联而不是偶然发现的可能性。这也表明 GJB2 基因可能在其他原因不明的 DWM 病例中起作用。

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