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

Batukan C., ÖZGÜN M. T., Basbug M., ÇAĞLAYAN A. O., DÜNDAR M., Murat N.

PRENATAL DIAGNOSIS, cilt.27, sa.4, ss.365-368, 2007 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 27 Sayı: 4
  • Basım Tarihi: 2007
  • Doi Numarası: 10.1002/pd.1653
  • Dergi Adı: PRENATAL DIAGNOSIS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.365-368
  • Anahtar Kelimeler: sacrococcygeal teratoma, distal 10q trisomy syndrome, facial dysmorphism, chromosomal anomaly, MILLER-DIEKER SYNDROME, 1Q
  • Dokuz Eylül Üniversitesi Adresli: Hayır

Özet

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.