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

Keywords

Sacrococcygeal Teratoma
Cornelia De Lange Syndrome
VATER Association

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

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.

https://doi.org/10.26440/IHRJ/0301.04.521069
PDF
HTML
EPUB
MOBI

Downloads

Download data is not yet available.