Title: Prenatal diagnosis of Prune Belly Syndrome in a case report
Authors: Sara.Boudhas, I traore, M.B Idrissi , N.Mamouni, S.Errarhay, C.Bouchikhi, A.Banani
Volume: 9
Issue: 2
Pages: 122-125
Publication Date: 2025/02/28
Abstract:
Prune Belly syndrome is a rare, predominantly male congenital malformation [1], characterised by a clinical triad of absent or hypoplastic abdominal muscles, cryptorchidism and urinary tract anomalies. In 75% of cases, it is associated with pulmonary, osteoarticular, cardiac and gastrointestinal malformations [2]. Prognosis depends essentially on urological involvement. We report a clinical case of Prune Belly syndrome diagnosed at the University Hospital of fes