{"title":"A “CHAR” Ming syndrome: Heart, bone, and eye","authors":"Anusha Mruthyunjayaswamy, Smitha Bhat","doi":"10.4103/ijhas.IJHAS_206_20","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":54094,"journal":{"name":"International Journal of Health and Allied Sciences","volume":"621 1","pages":"238 - 241"},"PeriodicalIF":0.0000,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Health and Allied Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ijhas.IJHAS_206_20","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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.