Prune belly syndrome associated with bilateral multicystic dysplastic kidneys and urethral obstruction: A case report

Arzu Akdag, Sule Arici, Betul Orhaner, Anil Dogan

Abstract


Prune belly syndrome is a rare congenital disorder defined by a characteristic
clinical triad: Abdominal muscle deficiency, severe urinary tract abnormalities,and bilateral cryptorchidism. We describe a preterm neonate of Prune Bellysyndrome who had abdominal muscle deficiency, multicystic dysplastic kidney,urethral hypoplasia and pulmonary hypoplasia. We presented this rare case withthe data gathered from the literature.

Keywords


Newborn; prune belly syndrome; pulmonary hypoplasia; multicystic dysplastic kidney; urethral obstruction.

Full Text:

PDF


DOI: http://dx.doi.org/10.14534/PUCR.2015410989

Refbacks

  • There are currently no refbacks.


Indexing/Abstracting

DOAJ, Tübitak/Ulakbim Turkish Medical Database, Academic OneFile, Health Reference Center Academic, US National Library of Medicine (NLM) Catalog, ICI Journals Master List (Index Copernicus), OCLC-WorldCat, Genamics-JournalSeek, J-Gate, Google Scholar, Ulrichsweb, CNKI Scholar, NAVER Academic, Research Bible, Cross Ref, EZB (Electronic Journals Library), JournalTOCs, HINARI, Norwegian Social Science Data Services (NSD), Turkiye Citation Index, SCIARY (Worldwide Science Educational Library), BASE (Bielefeld Academic Search Engine), NAIST, ICMJE, PubsHub, AcademicKeys, OAJI, OpenAIRE, Turk Medline, Publons, ROAD, SHERPA-ROMEO, SJFinder, Pubget, SciLit, Journal Finder, NYU Health Sciences Library, BIU Santé, Science Library Index, Ingenta Connect

Index Copernicus Value (ICV) 2018: 100.00

Pediatric Urology Case Reports journal does not charge a fee for submission, processing of manuscripts through peer-reviews, editing or publication of the articles.

Creative Commons License
Pediatric Urology Case Reports is licensed under a Creative Commons Attribution 4.0 International License.


eztekno