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病例报告:- 瑞典家族性指甲髌骨综合征的一个新病因及长期随访。

Case Report: Inversion of - A Novel Cause of Nail-Patella Syndrome in a Swedish Family and a Longtime Follow-Up.

机构信息

Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.

Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.

出版信息

Front Endocrinol (Lausanne). 2022 Jun 13;13:862908. doi: 10.3389/fendo.2022.862908. eCollection 2022.

Abstract

Nail-patella syndrome (NPS, OMIM #161200) is a rare autosomal dominant disorder with symptoms from many different parts of the body, including nails, knees, elbows, pelvis, kidneys and eyes. It is caused by truncating variants in the gene, which encodes a transcription factor with important roles during embryonic development, including dorsoventral patterning of the limbs. To our knowledge, inversions disrupting the gene have not been reported. Here, we report a family with an inversion disrupting the gene in five affected family members with mild but variable clinical features of NPS. Our finding demonstrates that genomic rearrangements must be considered a possible cause of NPS.

摘要

指甲髌骨综合征(NPS,OMIM #161200)是一种罕见的常染色体显性遗传病,其症状涉及身体的许多不同部位,包括指甲、膝盖、肘部、骨盆、肾脏和眼睛。它是由 基因突变引起的,该基因编码一种在胚胎发育过程中具有重要作用的转录因子,包括四肢的背腹模式形成。据我们所知, 基因的倒位尚未有报道。在这里,我们报告了一个家族,该家族的五个受累家庭成员存在 基因的倒位,具有轻度但可变的 NPS 临床特征。我们的发现表明,基因组重排必须被认为是 NPS 的一个可能原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a329/9235307/3b9f1308209f/fendo-13-862908-g001.jpg

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