PRENATALLY DIAGNOSED OBSTRUCTIVE UROPATHY IN A CASE WITH TRISOMY 13 IN A 16 WEEKS OLD FETUS

AYLA SARGIN, MİNE HATİPOĞLU, ZARİF YILMAZ, SERDAR CEYLANER, GÜLAY CEYLANER, BELGİN POLAT, MUSTAFA UĞUR

Gynecology Obstetrics & Reproductive Medicine - 2005;11(1):55-56

Zekai Tahir Burak Women's Health Education and Research Hospital, Ankara, Turkey

 

Abnormalities associated with trisomy 13 include holoprosencephaly, facial abnormalities of midline, polydactyly, congenital hearth defect, omphalocele and polycystic kidneys. Herein,we report the perinatal finding of a huge midline cystic bladder secondary to lower urinary tract obstruction associated with trisomy 13 in a male fetus. This case is a 41 years old multiparous woman; gravida 4, para 3, at 16 weeks pregnancy.Routine second trimester ultrasound scan revealed a distended bladder, lateral ventricular dilatation and bilateral hydronephrosis. Amniocentesis was performed and cytogenetic analysis revealed trisomy 13 (47, XY, +13). Pregnancy was terminated at 18 weeks with the informed consent of the family.Postmortem examination was not performed because the parents did not approve. Urethral obstruction is a rare finding in trisomy 13 but chromosomal anomalies occur in 23% of the fetuses with obstructive uropathy. Trisomies 18 and 13, del 2q, and 69XXY have been reported to occur in prenatally diagnosed obstructive uropathy.