{"title":"Mulvihill-Smith综合征1例报告","authors":"Kaori Yago , Taneaki Nakagawa , Tomoko Hyodo , Kenjiro Kosaki , Yusuke Kawata , Youichi Tanaka , Soichiro Asanami","doi":"10.1016/j.ajoms.2011.02.003","DOIUrl":null,"url":null,"abstract":"<div><p>Mulvihill–Smith syndrome (MSS) is a very rare disease that is characterized by short stature, a senile face with an under-developed lower half, microcephaly, multiple pigmented nevi, immunodeficiency, hearing loss, and high-pitched voice. We report on the oral manifestations and management of a 27-year-old woman with this syndrome, who underwent removal of a mandibular cyst and partial resection of the tongue.</p></div>","PeriodicalId":100128,"journal":{"name":"Asian Journal of Oral and Maxillofacial Surgery","volume":"23 4","pages":"Pages 186-190"},"PeriodicalIF":0.0000,"publicationDate":"2011-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.ajoms.2011.02.003","citationCount":"2","resultStr":"{\"title\":\"Mulvihill–Smith syndrome: A case report\",\"authors\":\"Kaori Yago , Taneaki Nakagawa , Tomoko Hyodo , Kenjiro Kosaki , Yusuke Kawata , Youichi Tanaka , Soichiro Asanami\",\"doi\":\"10.1016/j.ajoms.2011.02.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Mulvihill–Smith syndrome (MSS) is a very rare disease that is characterized by short stature, a senile face with an under-developed lower half, microcephaly, multiple pigmented nevi, immunodeficiency, hearing loss, and high-pitched voice. We report on the oral manifestations and management of a 27-year-old woman with this syndrome, who underwent removal of a mandibular cyst and partial resection of the tongue.</p></div>\",\"PeriodicalId\":100128,\"journal\":{\"name\":\"Asian Journal of Oral and Maxillofacial Surgery\",\"volume\":\"23 4\",\"pages\":\"Pages 186-190\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.ajoms.2011.02.003\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Oral and Maxillofacial Surgery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0915699211000264\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Oral and Maxillofacial Surgery","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0915699211000264","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Mulvihill–Smith syndrome (MSS) is a very rare disease that is characterized by short stature, a senile face with an under-developed lower half, microcephaly, multiple pigmented nevi, immunodeficiency, hearing loss, and high-pitched voice. We report on the oral manifestations and management of a 27-year-old woman with this syndrome, who underwent removal of a mandibular cyst and partial resection of the tongue.
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