@article{Seyed Reza Samsamshariat_2019, title={Sacrococcygeal Teratoma in a Singleton Male Instance of Cornelia de Lange Syndrome: A Case Report}, volume={3}, url={https://ihrjournal.com/ihrj/article/view/218}, DOI={10.26440/IHRJ/0301.04.521069}, abstractNote={<p>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.</p&gt;}, number={1}, journal={International Healthcare Research Journal}, author={Seyed Reza Samsamshariat}, year={2019}, month={Apr.}, pages={20-22} }