Open AccessSacrococcygeal Teratoma in a Singleton Male Instance of Cornelia de Lange Syndrome: A Case Report
Author(s) -
Seyed Reza Samsamshariat
Publication year - 2019
Publication title -
international healthcare research journal
Language(s) - English
Resource type - Journals
ISSN - 2456-8090
DOI - 10.26440/ihrj/0301.04.521069
Subject(s) - cornelia de lange syndrome , sacrococcygeal teratoma , anencephaly , medicine , teratoma , singleton , pregnancy , fetus , pediatrics , biology , surgery , genetics
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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