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血液学重要突变:施瓦赫曼-戴蒙德综合征。

Hematologically important mutations: Shwachman-Diamond syndrome.

作者信息

Costa Elísio, Santos Rosário

机构信息

Escola Superior de Saúde, Instituto Politécnico de Bragança, Avenida D. Afonso V, 5300-121 Bragança, Portugal.

出版信息

Blood Cells Mol Dis. 2008 Mar-Apr;40(2):183-4. doi: 10.1016/j.bcmd.2007.07.008. Epub 2007 Oct 4.

Abstract

Shwachman-Diamond syndrome (SDS) is a rare autosomal recessive disorder characterized by exocrine pancreatic insufficiency, bone marrow dysfunction, and skeletal abnormalities. The Shwachman-Bodian-Diamond syndrome (SBDS) gene was identified as a causative gene for SDS in 2003, and genetic analyses of SDS have been performed. Over the last 4 years, a number of different mutations affecting the SBDS gene have been described. In this report, a summary of documented SDS associated mutations is provided.

摘要

施瓦赫曼-戴蒙德综合征(SDS)是一种罕见的常染色体隐性疾病,其特征为外分泌胰腺功能不全、骨髓功能障碍和骨骼异常。2003年,施瓦赫曼-博迪安-戴蒙德综合征(SBDS)基因被确定为SDS的致病基因,并且已经对SDS进行了基因分析。在过去4年里,已经描述了许多影响SBDS基因的不同突变。在本报告中,提供了已记录的与SDS相关的突变的总结。

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