AI Summary & Key Takeaways
AI InsightPrune-Belly syndrome was reviewed with related literature and an usual case diagnosed at fetal ultrasonographic examination was presented.
📌 3 Key Takeaways
Abstract
Prune-Belly syndrome is characterized by deficient abdominal wall muscles, bilateral cryporchidism, and urinary tract abnormalities. A fetus was diagnosed with Prune-Belly syndrome by routine ultrasonographic examination at 29th gestational week. Although various degrees of renal involvement occur in Prune-Belly syndrome, renal dysplasia is the major determinant of fetal survival and postnatal prognosis. Prune-Belly syndrome was reviewed with related literature and an usual case diagnosed at fetal ultrasonographic examination was presented.
Özet
Prune-Belly sendromu karın kaslarının yokluğu, bilateral inmemiş testis ve üriner sistem anomalileri ile karakterize bir sendromdur. İntrauterin dönemde 29 haftalık bir fetusta rutin ultrasonografik inceleme sırasında Prune-Belly sendromu düşünüldü. Prune-Belly sendromunda çeşitli derecede renal tutulum olsa da, fetal ve postnatal prognozu belirlemede major faktör renal displazidir. Doğumdan sonra tanısı kesinleştirilen olgu literatür bilgileri eşliğinde sunuldu.