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Rare urogenital malformation with prune belly syndrome in a newborn female: a case report
Publication type: Journal Article
Publication date: 2025-04-01
scimago Q4
wos Q4
SJR: 0.158
CiteScore: 0.6
Impact factor: 0.2
ISSN: 22135766
Abstract
IntroductionPrune Belly syndrome (PBS) is a rare congenital anomaly almost exclusive to males. It includes a triad of urinary tract abnormality, lack of abdominal muscles, and cryptorchidism. Urorectal septum malformation sequence (URSMS) is an even more rare congenital anomaly defined by the presence of ambiguous genitalia, absent perineal openings, and lumbosacral abnormalities. The association of PBS and elements of URSMS in a female patient is extremely rare.
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Elhafid M., Milbrandt K. Rare urogenital malformation with prune belly syndrome in a newborn female: a case report // Journal of Pediatric Surgery Case Reports. 2025. Vol. 115. p. 102973.
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Elhafid M., Milbrandt K. Rare urogenital malformation with prune belly syndrome in a newborn female: a case report // Journal of Pediatric Surgery Case Reports. 2025. Vol. 115. p. 102973.
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TY - JOUR
DO - 10.1016/j.epsc.2025.102973
UR - https://linkinghub.elsevier.com/retrieve/pii/S2213576625000181
TI - Rare urogenital malformation with prune belly syndrome in a newborn female: a case report
T2 - Journal of Pediatric Surgery Case Reports
AU - Elhafid, Melanie
AU - Milbrandt, Kristopher
PY - 2025
DA - 2025/04/01
PB - Elsevier
SP - 102973
VL - 115
SN - 2213-5766
ER -
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@article{2025_Elhafid,
author = {Melanie Elhafid and Kristopher Milbrandt},
title = {Rare urogenital malformation with prune belly syndrome in a newborn female: a case report},
journal = {Journal of Pediatric Surgery Case Reports},
year = {2025},
volume = {115},
publisher = {Elsevier},
month = {apr},
url = {https://linkinghub.elsevier.com/retrieve/pii/S2213576625000181},
pages = {102973},
doi = {10.1016/j.epsc.2025.102973}
}