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Persistent Mullerian duct syndrome with polycystic ovary in a young adult: A rare case report
Persistent Mullerian Duct Syndrome (PMDS) is a type of pseudohermaphroditism that occurs in males. It is an autosomal recessive type of familial disease that is commonly associated with a history of consanguinity. We have documented this case of a 22-year-old adult male who came with acute right ili...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008828/ https://www.ncbi.nlm.nih.gov/pubmed/36923385 http://dx.doi.org/10.1016/j.radcr.2023.02.015 |
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author | Hamd, Zuhal Y. Ali, Muthab A. Mohammed Alorainy, Amal I. Gareeballah, Awadia Hamdoun, Anas Manssor, E. Alhomida, Basim Abdullah. |
author_facet | Hamd, Zuhal Y. Ali, Muthab A. Mohammed Alorainy, Amal I. Gareeballah, Awadia Hamdoun, Anas Manssor, E. Alhomida, Basim Abdullah. |
author_sort | Hamd, Zuhal Y. |
collection | PubMed |
description | Persistent Mullerian Duct Syndrome (PMDS) is a type of pseudohermaphroditism that occurs in males. It is an autosomal recessive type of familial disease that is commonly associated with a history of consanguinity. We have documented this case of a 22-year-old adult male who came with acute right iliac pain; after an ultrasound scan and hormone investigations, he was diagnosed with polycystic ovarian syndrome (PCOS). |
format | Online Article Text |
id | pubmed-10008828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-100088282023-03-14 Persistent Mullerian duct syndrome with polycystic ovary in a young adult: A rare case report Hamd, Zuhal Y. Ali, Muthab A. Mohammed Alorainy, Amal I. Gareeballah, Awadia Hamdoun, Anas Manssor, E. Alhomida, Basim Abdullah. Radiol Case Rep Case Report Persistent Mullerian Duct Syndrome (PMDS) is a type of pseudohermaphroditism that occurs in males. It is an autosomal recessive type of familial disease that is commonly associated with a history of consanguinity. We have documented this case of a 22-year-old adult male who came with acute right iliac pain; after an ultrasound scan and hormone investigations, he was diagnosed with polycystic ovarian syndrome (PCOS). Elsevier 2023-03-05 /pmc/articles/PMC10008828/ /pubmed/36923385 http://dx.doi.org/10.1016/j.radcr.2023.02.015 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Hamd, Zuhal Y. Ali, Muthab A. Mohammed Alorainy, Amal I. Gareeballah, Awadia Hamdoun, Anas Manssor, E. Alhomida, Basim Abdullah. Persistent Mullerian duct syndrome with polycystic ovary in a young adult: A rare case report |
title | Persistent Mullerian duct syndrome with polycystic ovary in a young adult: A rare case report |
title_full | Persistent Mullerian duct syndrome with polycystic ovary in a young adult: A rare case report |
title_fullStr | Persistent Mullerian duct syndrome with polycystic ovary in a young adult: A rare case report |
title_full_unstemmed | Persistent Mullerian duct syndrome with polycystic ovary in a young adult: A rare case report |
title_short | Persistent Mullerian duct syndrome with polycystic ovary in a young adult: A rare case report |
title_sort | persistent mullerian duct syndrome with polycystic ovary in a young adult: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008828/ https://www.ncbi.nlm.nih.gov/pubmed/36923385 http://dx.doi.org/10.1016/j.radcr.2023.02.015 |
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