{"title":"Variable expression of Van der Woude syndrome in the same family","authors":"R. Mahajan, Sheikh Ali, Sana Jameel, Samik Sharma","doi":"10.4103/jclpca.jclpca_9_21","DOIUrl":null,"url":null,"abstract":"Van der Woude syndrome is a rare congenital condition with autosomal dominant traits. This autosomal dominant syndrome had been reported to have a penetrance of 80% with variable expression.[1] This genetic disorder is characterized by the combination of lip pits, cleft lip with or without cleft palate, and cleft palate only. Even within the families, there is a wide variability of affected gene expressions. It is very important to establish the correct diagnosis so that genetic counseling can be recommended in such cases. Here, we report cases of Van der Woude syndrome in the same family having the same genetic inheritance with variable expression.","PeriodicalId":34294,"journal":{"name":"Journal of Cleft Lip Palate and Craniofacial Anomalies","volume":"9 1","pages":"74 - 77"},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cleft Lip Palate and Craniofacial Anomalies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/jclpca.jclpca_9_21","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
Van der Woude syndrome is a rare congenital condition with autosomal dominant traits. This autosomal dominant syndrome had been reported to have a penetrance of 80% with variable expression.[1] This genetic disorder is characterized by the combination of lip pits, cleft lip with or without cleft palate, and cleft palate only. Even within the families, there is a wide variability of affected gene expressions. It is very important to establish the correct diagnosis so that genetic counseling can be recommended in such cases. Here, we report cases of Van der Woude syndrome in the same family having the same genetic inheritance with variable expression.
Van der Woude综合征是一种罕见的先天性疾病,具有常染色体显性特征。据报道,这种常染色体显性综合征的外显率为80%,表达可变这种遗传疾病的特征是唇窝,唇裂伴或不伴腭裂,以及只有腭裂。即使在家族内部,受影响的基因表达也存在很大的差异。建立正确的诊断是非常重要的,这样在这种情况下可以推荐遗传咨询。在这里,我们报告了同一家族中具有相同基因遗传但表达不同的范德沃德综合征病例。