K. Murray, Kahleb Graham, S. Szabo, S. Kocoshis, Lev, Dorfman, A. Kaul
{"title":"Spectrum of Congenital Myenteric Hypoganglionosis and Aganglionosis in Patients with Waardenburg Syndrome Type 4","authors":"K. Murray, Kahleb Graham, S. Szabo, S. Kocoshis, Lev, Dorfman, A. Kaul","doi":"10.29011/2575-825x.100268","DOIUrl":null,"url":null,"abstract":"Introduction: Waardenburg Syndrome (WS) is a rare, genetically and phenotypically heterogeneous disorder caused by abnormal migration or differentiation of neural crest cells during embryonic development. WS is classified into four types: WS Type 1 (WS1), WS2, WS3","PeriodicalId":8302,"journal":{"name":"Archives of pediatrics","volume":"89 1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of pediatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29011/2575-825x.100268","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract
Introduction: Waardenburg Syndrome (WS) is a rare, genetically and phenotypically heterogeneous disorder caused by abnormal migration or differentiation of neural crest cells during embryonic development. WS is classified into four types: WS Type 1 (WS1), WS2, WS3
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