Y Alembik, D Christmann, A de Saint Martin, M Eliot, H Dollfus, F Pauly, C Stoll
{"title":"Schinzel-Giedion syndrome with severe deafness and neurodegenerative process.","authors":"Y Alembik, D Christmann, A de Saint Martin, M Eliot, H Dollfus, F Pauly, C Stoll","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>A case of Schinzel-Giedion syndrome with a follow-up of two and a half years is reported. In addition to the classical features of the syndrome, the patient had severe hearing loss with ossicular and cochlear malformations, alacrymia, and progressive neurodegenerative disease.</p>","PeriodicalId":7908,"journal":{"name":"Annales de genetique","volume":"42 4","pages":"225-30"},"PeriodicalIF":0.0000,"publicationDate":"1999-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annales de genetique","FirstCategoryId":"1085","ListUrlMain":"","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
A case of Schinzel-Giedion syndrome with a follow-up of two and a half years is reported. In addition to the classical features of the syndrome, the patient had severe hearing loss with ossicular and cochlear malformations, alacrymia, and progressive neurodegenerative disease.