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Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia
Persistent Mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism characterized by the presence of Mullerian duct structures in a normal male with 46, XY karyotype. Transverse testicular ectopia (TTE) is rare form of testicular ectopia in which two testes are located on one ingu...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959409/ https://www.ncbi.nlm.nih.gov/pubmed/27512542 http://dx.doi.org/10.4103/2006-8808.184940 |
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author | Kumar, P. Naresh Venugopala, Kandgal |
author_facet | Kumar, P. Naresh Venugopala, Kandgal |
author_sort | Kumar, P. Naresh |
collection | PubMed |
description | Persistent Mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism characterized by the presence of Mullerian duct structures in a normal male with 46, XY karyotype. Transverse testicular ectopia (TTE) is rare form of testicular ectopia in which two testes are located on one inguinal side. The opposite scrotum is empty. PMDS with TTE is rare. We report a case of PMDS with TTE discovered during surgery for a right inguinal hernia in a 25-year-old male. |
format | Online Article Text |
id | pubmed-4959409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49594092016-08-10 Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia Kumar, P. Naresh Venugopala, Kandgal J Surg Tech Case Rep Case Report Persistent Mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism characterized by the presence of Mullerian duct structures in a normal male with 46, XY karyotype. Transverse testicular ectopia (TTE) is rare form of testicular ectopia in which two testes are located on one inguinal side. The opposite scrotum is empty. PMDS with TTE is rare. We report a case of PMDS with TTE discovered during surgery for a right inguinal hernia in a 25-year-old male. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4959409/ /pubmed/27512542 http://dx.doi.org/10.4103/2006-8808.184940 Text en Copyright: © Journal of Surgical Technique and Case Report 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Kumar, P. Naresh Venugopala, Kandgal Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia |
title | Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia |
title_full | Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia |
title_fullStr | Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia |
title_full_unstemmed | Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia |
title_short | Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia |
title_sort | persistent mullerian duct syndrome with transverse testicular ectopia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959409/ https://www.ncbi.nlm.nih.gov/pubmed/27512542 http://dx.doi.org/10.4103/2006-8808.184940 |
work_keys_str_mv | AT kumarpnaresh persistentmullerianductsyndromewithtransversetesticularectopia AT venugopalakandgal persistentmullerianductsyndromewithtransversetesticularectopia |