Sacrococcygeal teratoma in a fetus with prenatally diagnosed partial trisomy 10q (10q24.3 -> qter) and partial monosomy 17p (p13.3 -> pter)


BATUKAN C., Ozgun M. T. , Basbug M. , ÇAĞLAYAN O., Dundar M. , Murat N.

PRENATAL DIAGNOSIS, vol.27, no.4, pp.365-368, 2007 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 27 Issue: 4
  • Publication Date: 2007
  • Doi Number: 10.1002/pd.1653
  • Title of Journal : PRENATAL DIAGNOSIS
  • Page Numbers: pp.365-368

Abstract

Objective Clinical features of the distal 10q trisomy syndrome consist of mental retardation, facial dysmorphism and renal and cardiac anomalies. The presence of a sacrococcygeal teratoma (SCT) in a fetus with distal 10q trisomy has not been reported yet.