K. Murray, Kahleb Graham, S. Szabo, S. Kocoshis, Lev, Dorfman, A. Kaul
{"title":"Waardenburg综合征4型患者先天性肌enteric神经节减少症和Aganglionosis的谱","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":"{\"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}","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}
Spectrum of Congenital Myenteric Hypoganglionosis and Aganglionosis in Patients with Waardenburg Syndrome Type 4
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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