Suppr超能文献

克里斯波尼/ CISS1综合征:病例系列

Crisponi/CISS1 syndrome: A case series.

作者信息

Alhashem Amal M, Majeed-Saidan Muhammad Ali, Ammari Amer N, Alrakaf Maha S, Nojoom Maha, Maddirevula Sateesh, Faqeih Eissa, Alkuraya Fowzan S, Garne Ester, Kurdi Ahmad M

机构信息

Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.

Department of Medical Services-Birth Defect Registry (MSD-BDR) Office, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.

出版信息

Am J Med Genet A. 2016 May;170A(5):1236-41. doi: 10.1002/ajmg.a.37569. Epub 2016 Jan 24.

Abstract

Crisponi/CISS1 syndrome (MIM#272430) is a rare autosomal recessive disease characterized by major feeding difficulties, camptodactyly, and anhidrosis in early childhood; and the subsequent development of paradoxical cold-induced sweating and scoliosis later in life. The syndrome is caused by biallelic mutations in CRLF1 or, much less commonly, CLCF1. Although genotype/phenotype correlation has been elusive, it has been suggested that the level of the mutant protein may correlate with the phenotypic severity. However, we show in this series of 12 patients from four families, all previously unpublished, that the homogeneity of the recently described c.983dupG (p.Ser328Argfs∗2) mutation in CRLF1 was associated with a highly variable degree of severity, and that the phenotype significantly overlaps with the recently described COG6-related anhidrosis syndrome (MIM#615328). Another fifth previously unpublished family is also described with a novel mutation in CRLF1, c.605delC (p.Ala202Valfs*32). In Saudi Arabia the prevalence of the syndrome is probably underestimated due to the difficulty in making the diagnosis considering the complex phenotype with typical neonatal and evolutive features.

摘要

克里斯波尼/ CISS1综合征(MIM#272430)是一种罕见的常染色体隐性疾病,其特征为幼儿期出现严重喂养困难、屈曲指和无汗症;以及在生命后期出现反常的冷诱导出汗和脊柱侧弯。该综合征由CRLF1基因的双等位基因突变引起,较少见的是由CLCF1基因突变引起。尽管基因型/表型的相关性尚不明确,但有人提出突变蛋白的水平可能与表型严重程度相关。然而,我们在来自四个家族的这一系列12例患者(此前均未发表)中发现,CRLF1基因中最近描述的c.983dupG(p.Ser328Argfs∗2)突变的同质性与高度可变的严重程度相关,并且该表型与最近描述的COG6相关无汗症综合征(MIM#615328)有显著重叠。还描述了另一个此前未发表的第五个家族,其CRLF1基因存在新突变c.605delC(p.Ala202Valfs*32)。在沙特阿拉伯,由于考虑到具有典型新生儿和演变特征的复杂表型而难以做出诊断,该综合征的患病率可能被低估。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验