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埃利斯-范克里维尔德综合征:一例报告。

Ellis-van Creveld syndrome: a case report.

作者信息

Shah B, Ashok L, Sujatha G P

机构信息

Department of Oral Medicine and Radiology, Bapuji Dental College and Hospital, Davangere 577 004, Karnataka, India.

出版信息

J Indian Soc Pedod Prev Dent. 2008 Jan;26 Suppl 1:S19-22.

Abstract

Ellis-van Creveld syndrome (EvC) is a disease complex, where all the three embryonic layers appear to be involved. This disorder is also called as Chondroectodermal dysplasia. EvC is an autosomal recessive disorder resulting from mutations in these patients. Mutations in the two genes EVC and EVC2, have been identified to cause the condition. It has been considered as a skeletal dysplasia with an incidence of approximately 1 out of 1,50,000 live births. A high prevalence has been reported among certain populations like Amish and Arabs of Gaza strip. There are more than 300 cases of EvC reported into the literature. About 50-60% of cases have been reported with congenital cardiac malformations.

摘要

埃利斯-范克里维尔德综合征(EvC)是一种复杂的疾病,似乎所有三个胚层都受到影响。这种病症也被称为软骨外胚层发育不良。EvC是一种常染色体隐性疾病,由这些患者的基因突变引起。已确定EVC和EVC2这两个基因的突变会导致该病。它被认为是一种骨骼发育不良,发病率约为每15万例活产中有1例。据报道,在某些人群中,如阿米什人和加沙地带的阿拉伯人,其患病率较高。文献中已报道了300多例EvC病例。约50-60%的病例伴有先天性心脏畸形。

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