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PRG4基因的一种新型突变是先天性屈曲挛缩-关节病-髋内翻-心包炎综合征的潜在病因,其表型可能扩展至包括先天性白内障。

A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.

作者信息

Akawi Nadia A, Ali Bassam R, Al-Gazali Lihadh

机构信息

Department of Pathology, Faculty of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.

出版信息

Birth Defects Res A Clin Mol Teratol. 2012 Jul;94(7):553-6. doi: 10.1002/bdra.23031. Epub 2012 Jun 8.

Abstract

BACKGROUND

Camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is a clinically heterogenous congenital disorder caused by mutations in proteoglycan 4 (PRG4), a chondroitin sulfate proteoglycan that acts as a lubricant for the cartilage surface. Although CACP is a rare genetic disorder, several cases were described in the literature from ethnically different populations including Caucasian, Egyptian, Saudi Arabian, Pakistani, and Korean. We report CACP for the first time in United Arab Emirates.

METHODS

Direct sequencing of all the coding exons and splice sites of the PRG4 gene was performed for all the members of the affected family.

RESULTS

The studied family is consanguineous and has multiple affected members from different branches showing congenital camptodactyly with arthropathy, the hallmarks of CACP. All the affected family members lack pericarditis, but one of them was born with cataract, which has never been documented in any of the previously reported cases of CACP. Molecular analysis revealed a novel homozygous insertion of a cytosine nucleotide (c.1320dupC) in the highly repetitive portion of the coding sequence of the PRG4 gene. The detected mutation caused a frameshift in the cDNA sequence and created a premature termination codon (p.P440fsX197), which is likely to result in a nonfunctional protein.

CONCLUSION

We report a family from the United Arab Emirates with typical features of CACP in whom one of the children had in addition, a bilateral congenital cataract. We also report the identification of a novel null mutation in PRG4 confirming the genetic homogeneity of CACP.

摘要

背景

屈曲指-关节病-髋内翻-心包炎综合征(CACP)是一种临床异质性先天性疾病,由蛋白聚糖4(PRG4)突变引起,PRG4是一种硫酸软骨素蛋白聚糖,可作为软骨表面的润滑剂。尽管CACP是一种罕见的遗传疾病,但文献中描述了来自不同种族人群的几例病例,包括白种人、埃及人、沙特阿拉伯人、巴基斯坦人和韩国人。我们首次在阿拉伯联合酋长国报告了CACP。

方法

对受影响家族的所有成员进行PRG4基因所有编码外显子和剪接位点的直接测序。

结果

所研究的家族是近亲家族,不同分支中有多个受影响成员,表现出先天性屈曲指伴关节病,这是CACP的特征。所有受影响的家族成员均无心包炎,但其中一人出生时患有白内障,这在之前报道的任何CACP病例中均未记录。分子分析显示,PRG4基因编码序列的高度重复部分存在一个新的胞嘧啶核苷酸纯合插入(c.1320dupC)。检测到的突变导致cDNA序列发生移码,并产生一个提前终止密码子(p.P440fsX197),这可能导致产生无功能的蛋白质。

结论

我们报告了一个来自阿拉伯联合酋长国的家族,具有CACP的典型特征,其中一个孩子还患有双侧先天性白内障。我们还报告了在PRG4中鉴定出一种新的无效突变,证实了CACP的遗传同质性。

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