A case of Prune-belly syndrome associated with multiple congenital anomalies Multipl konjenital anomalilerin eslik ettigi bir Prune-belly sendromu olgusu
Ondokuz Mayis Universitesi Tip Dergisi, cilt.15, sa.4, ss.330-334, 1998 (Scopus, TRDizin)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 15 Sayı: 4
- Basım Tarihi: 1998
- Dergi Adı: Ondokuz Mayis Universitesi Tip Dergisi
- Derginin Tarandığı İndeksler: Scopus, TR DİZİN (ULAKBİM)
- Sayfa Sayıları: ss.330-334
- Anahtar Kelimeler: Multiple congenital anomalies, Prune-belly syndrome
- Ondokuz Mayıs Üniversitesi Adresli: Evet
Özet
Abdominal muscle deficiency, urinary tract abnormalities and cryptoorchidism are the three major features of the Prune-belly syndrome. Massive acites and intraabdominal urine accumination had produced abdominal wall atrophy. A functional or anatomic urethral obstruction may detect on cases. As an addition classic triad of Prune-belly syndrome our case has polydactily, cleft lip and palate. Chromosomal analysis could not be done our cases due to in utero exitus.