Sacrococcygeal Teratoma in a Singleton Male Instance of Cornelia de Lange Syndrome: A Case Report

  • Seyed Reza Samsamshariat
Keywords: Sacrococcygeal Teratoma, Cornelia De Lange Syndrome, VATER Association

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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Author Biography

Seyed Reza Samsamshariat

MD, Pathologist
Dr. Samsamshariat Clinical and Surgical Pathology Laboratory
Khorasgan, Esfahan, Iran

Published
2019-04-17
How to Cite
Seyed Reza Samsamshariat. (2019). Sacrococcygeal Teratoma in a Singleton Male Instance of Cornelia de Lange Syndrome: A Case Report. International Healthcare Research Journal, 3(1), 20-22. https://doi.org/10.26440/IHRJ/0301.04.521069