PRUNE BELLY SYNDROME: A CASE REPORT

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Autore principale: Fatima Mbarki , Khadija Skalli , Driss Oukachou and Fouzia Hmami
Natura: Recurso digital
Pubblicazione: Zenodo 2025
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author Fatima Mbarki , Khadija Skalli , Driss Oukachou and Fouzia Hmami
author_facet Fatima Mbarki , Khadija Skalli , Driss Oukachou and Fouzia Hmami
contents <p>Prune Belly Syndrome (PBS) is a rare congenital malformation that primarily affects boys. It is characterized by hypoplasia of the abdominal wall muscles, urological anomalies, and bilateral cryptorchidism. Although the etiology remains unclear, genetic factors and chromosomal abnormalities are suspected. Early diagnosis is essential, as the prognosis ranges from unfavorable to near-normal survival. We report the case of a premature neonate diagnosed with PBS at birth, who required surgical intervention but unfortunately passed away at 8 months due to urinary tract infections and severe dehydration. A multidisciplinaryapproachis crucial to improve patient outcomes.</p> <p> </p>
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spellingShingle PRUNE BELLY SYNDROME: A CASE REPORT
Fatima Mbarki , Khadija Skalli , Driss Oukachou and Fouzia Hmami
Prune Belly Syndrome Abdominal Wall Musculature Deficiency Bilateral Cryptorchidism Urinary Tract Anomalies
<p>Prune Belly Syndrome (PBS) is a rare congenital malformation that primarily affects boys. It is characterized by hypoplasia of the abdominal wall muscles, urological anomalies, and bilateral cryptorchidism. Although the etiology remains unclear, genetic factors and chromosomal abnormalities are suspected. Early diagnosis is essential, as the prognosis ranges from unfavorable to near-normal survival. We report the case of a premature neonate diagnosed with PBS at birth, who required surgical intervention but unfortunately passed away at 8 months due to urinary tract infections and severe dehydration. A multidisciplinaryapproachis crucial to improve patient outcomes.</p> <p> </p>
title PRUNE BELLY SYNDROME: A CASE REPORT
topic Prune Belly Syndrome Abdominal Wall Musculature Deficiency Bilateral Cryptorchidism Urinary Tract Anomalies
url https://doi.org/10.21474/IJAR01/20447