An extremely rare case of classic complete caudal duplication: Dipygus

Dipygus is a complete caudal duplication deformity in its severest form. The structures derived from the embryonic cloaca and notochords are duplicated to various extent. We report a male baby who presented to us with complete somatic and visceral duplication below the umbilical level associated wit...

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Autores principales: Al Alayet, Yasen Fayez, Samujh, Ram, Lyngdoh, Toijam Soni, Mansoor, Khizer, Al Kasim, Fawaz, Al-Mustafa, Abdulaziz A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155636/
https://www.ncbi.nlm.nih.gov/pubmed/25197197
http://dx.doi.org/10.4103/0971-9261.136478
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author Al Alayet, Yasen Fayez
Samujh, Ram
Lyngdoh, Toijam Soni
Mansoor, Khizer
Al Kasim, Fawaz
Al-Mustafa, Abdulaziz A.
author_facet Al Alayet, Yasen Fayez
Samujh, Ram
Lyngdoh, Toijam Soni
Mansoor, Khizer
Al Kasim, Fawaz
Al-Mustafa, Abdulaziz A.
author_sort Al Alayet, Yasen Fayez
collection PubMed
description Dipygus is a complete caudal duplication deformity in its severest form. The structures derived from the embryonic cloaca and notochords are duplicated to various extent. We report a male baby who presented to us with complete somatic and visceral duplication below the umbilical level associated with gastroschisis and imperforated anus. Staged surgical corrections were suggested and three out of the four stages were performed successfully.
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spelling pubmed-41556362014-09-05 An extremely rare case of classic complete caudal duplication: Dipygus Al Alayet, Yasen Fayez Samujh, Ram Lyngdoh, Toijam Soni Mansoor, Khizer Al Kasim, Fawaz Al-Mustafa, Abdulaziz A. J Indian Assoc Pediatr Surg Case Report Dipygus is a complete caudal duplication deformity in its severest form. The structures derived from the embryonic cloaca and notochords are duplicated to various extent. We report a male baby who presented to us with complete somatic and visceral duplication below the umbilical level associated with gastroschisis and imperforated anus. Staged surgical corrections were suggested and three out of the four stages were performed successfully. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4155636/ /pubmed/25197197 http://dx.doi.org/10.4103/0971-9261.136478 Text en Copyright: © Journal of Indian Association of Pediatric Surgeons http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Al Alayet, Yasen Fayez
Samujh, Ram
Lyngdoh, Toijam Soni
Mansoor, Khizer
Al Kasim, Fawaz
Al-Mustafa, Abdulaziz A.
An extremely rare case of classic complete caudal duplication: Dipygus
title An extremely rare case of classic complete caudal duplication: Dipygus
title_full An extremely rare case of classic complete caudal duplication: Dipygus
title_fullStr An extremely rare case of classic complete caudal duplication: Dipygus
title_full_unstemmed An extremely rare case of classic complete caudal duplication: Dipygus
title_short An extremely rare case of classic complete caudal duplication: Dipygus
title_sort extremely rare case of classic complete caudal duplication: dipygus
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155636/
https://www.ncbi.nlm.nih.gov/pubmed/25197197
http://dx.doi.org/10.4103/0971-9261.136478
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