Sacrococcygeal Teratoma in a Singleton Male Instance of Cornelia de Lange Syndrome: A Case Report
2019 ◽
Vol 3
(1)
◽
pp. 20-22
Keyword(s):
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.
2019 ◽
Vol 3
(1)
◽
pp. 20-22
1990 ◽
Vol 25
(2)
◽
pp. 591
2016 ◽
Vol 16
(1-2)
◽
pp. 61-69
◽
Keyword(s):
2020 ◽
Vol 41
(1)
◽
pp. 30-31
2012 ◽
Vol 1
(4)
◽
pp. 268
Keyword(s):
Keyword(s):