“CHAR”明综合征:心脏、骨骼和眼睛

Anusha Mruthyunjayaswamy, Smitha Bhat
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引用次数: 0

摘要

心脏病是常见的先天性异常,发病率为每1000例活产8-12例。一些遗传综合征与特定的心脏异常有关,Char是第一个描述了一种与动脉导管未闭(PDA)和各种特征相关的综合征,包括中短、鸭嘴、上睑下垂、低耳和手脚的第五指短。在这里,我们报告一个20岁男性的病例,他表现为三联综合征,即PDA伴分流逆转,面部畸形和骨骼异常。此外,他有先天性耳聋和双眼虹膜缺损,这是一种罕见的关联,迄今为止从未报道过。Char综合征很少见;全世界只报告了少数病例,我们区域几乎没有报告病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A “CHAR” Ming syndrome: Heart, bone, and eye
Heart diseases are common congenital anomalies, with a prevalence of 8–12 per 1000 live births. Several genetic syndromes are associated with specific cardiac anomalies and Char was the first to describe a syndrome associated with patent ductus arteriosus (PDA) and various features, including a short philtrum, duck bill lips, ptosis, low set ears, and short fifth digits in both hands and feet. Here, we report a case of a 20-year-old male who presented with the triad of char syndrome, that is, a PDA with a shunt reversal, facial dysmorphism, and skeletal abnormalities. Additionally, he had congenital deafness and both eyes iris coloboma, a rare association which has never been reported so far. Char syndrome is rare; only a few cases have been reported worldwide, and almost none from our region.
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