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A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency

Aphallia or penile agenesis is a rare congenital malformation with an estimated incidence rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated anomalies including caudal axis, cardiovascular, genitourinary, and gastrointestinal anomalies. The penile agenesis associa...

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Autores principales: El Qadiry, R., Lalaoui, A., Nassih, H., Bourrahouat, A., Ait Sab, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7704127/
https://www.ncbi.nlm.nih.gov/pubmed/33299630
http://dx.doi.org/10.1155/2020/8826520
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author El Qadiry, R.
Lalaoui, A.
Nassih, H.
Bourrahouat, A.
Ait Sab, I.
author_facet El Qadiry, R.
Lalaoui, A.
Nassih, H.
Bourrahouat, A.
Ait Sab, I.
author_sort El Qadiry, R.
collection PubMed
description Aphallia or penile agenesis is a rare congenital malformation with an estimated incidence rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated anomalies including caudal axis, cardiovascular, genitourinary, and gastrointestinal anomalies. The penile agenesis associated with adrenal insufficiency has never been reported in an infant. We report a rare case of a newborn that was diagnosed as a case of aphallia with vesicorectal fistula and vesicoureteral reflux, complicated by adrenal insufficiency with salt-wasting crisis.
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spelling pubmed-77041272020-12-08 A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency El Qadiry, R. Lalaoui, A. Nassih, H. Bourrahouat, A. Ait Sab, I. Case Rep Pediatr Case Report Aphallia or penile agenesis is a rare congenital malformation with an estimated incidence rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated anomalies including caudal axis, cardiovascular, genitourinary, and gastrointestinal anomalies. The penile agenesis associated with adrenal insufficiency has never been reported in an infant. We report a rare case of a newborn that was diagnosed as a case of aphallia with vesicorectal fistula and vesicoureteral reflux, complicated by adrenal insufficiency with salt-wasting crisis. Hindawi 2020-11-23 /pmc/articles/PMC7704127/ /pubmed/33299630 http://dx.doi.org/10.1155/2020/8826520 Text en Copyright © 2020 R. El Qadiry et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
El Qadiry, R.
Lalaoui, A.
Nassih, H.
Bourrahouat, A.
Ait Sab, I.
A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
title A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
title_full A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
title_fullStr A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
title_full_unstemmed A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
title_short A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
title_sort new presentation: aphallia, vesicoureteral reflux, rectovesical fistula, and adrenal insufficiency
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7704127/
https://www.ncbi.nlm.nih.gov/pubmed/33299630
http://dx.doi.org/10.1155/2020/8826520
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