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Sacrococcygeal Teratoma in a Singleton Male Instance of Cornelia de Lange Syndrome: A Case Report
Journal: International Healthcare Research Journal (Vol.3, No. 1)Publication Date: 2019-04-19
Authors : Seyed Reza Samsamshariat;
Page : 20-22
Keywords : Sacrococcygeal Teratoma; Cornelia De Lange Syndrome; VATER Association;
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Abstract
Sacrococcygeal teratoma, sirenomelia, VATER association, anencephaly and holoprocencephaly are occasionally observed in patients with Cornelia de Lange syndrome (CdLS; OMIM 122470). Here, I present an exceptional case of a non-twin, singleton newborn with CdLs who also had a sacrococcygeal teratoma.
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Last modified: 2019-07-06 15:16:44