Multipl Konjenital Anomalilerin Eşlik Ettiği Bir Prune-Belly Sendromu Olgusu

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Journal of Experimental and Clinical Medicine
Volume:15 Issue:4
Multipl Konjenital Anomalilerin Eşlik Ettiği Bir Prune-Belly Sendromu Olgusu

Multipl Konjenital Anomalilerin Eşlik Ettiği Bir Prune-Belly Sendromu Olgusu

Authors : L YILDIZ, O AYDIN, Ç BORAN, B KANDEMİR, T ALPER

Pages : 0-0

Doi:10.5835/jecm.v15i4.816

View : 41 | Download : 16

Publication Date : 2009-12-23

Article Type : Other Papers

Abstract :A Case of Prune-Belly Syndrome Associated with Multiple Congenital Anomalies Abdominal muscle deficiency, urinary tract abnormalities and cryptoorchidism are the three major features of the Prune-belly syndrome. Massive acites and intraabdominal urine accumulation 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. Karın duvarı kaslarının yokluğu, üriner traktus anormallikleri ve kriptoorşitizm Prune-belly sendromunun üç ana özelliğidir. Yoğun asit ve intraabdominal idrar birikimi abdominal duvar atrofisine yol açar. Olgularda fonksiyonel ya da anatomik üretral obstrüksiyon tespit edilebilir. Bizim olgumuzda Prune-belly sendromunun klasik triadma ek olarak polidaktili, yarık damak ve dudak mevcuttu. Olgu in utero eksitus olduğundan kromozom analizi yapılamadı.
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