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46,XX Male Disorder of Sexual Development: A Case Report

The main factor influencing sex determination of an embryo is the sex-determining region Y (SRY), a master regulatory gene located on the Y chromosome. The presence of SRY causes the bipotential gonad to differentiate into a testis. However, some individuals carry a Y chromosome but are phenotypical...

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Detalles Bibliográficos
Autores principales: Anık, Ahmet, Çatlı, Gönül, Abacı, Ayhan, Böber, Ece
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890225/
https://www.ncbi.nlm.nih.gov/pubmed/24379036
http://dx.doi.org/10.4274/Jcrpe.1098
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author Anık, Ahmet
Çatlı, Gönül
Abacı, Ayhan
Böber, Ece
author_facet Anık, Ahmet
Çatlı, Gönül
Abacı, Ayhan
Böber, Ece
author_sort Anık, Ahmet
collection PubMed
description The main factor influencing sex determination of an embryo is the sex-determining region Y (SRY), a master regulatory gene located on the Y chromosome. The presence of SRY causes the bipotential gonad to differentiate into a testis. However, some individuals carry a Y chromosome but are phenotypically female (46,XY females) or have a female karyotype but are phenotypically male (46,XX males). 46, XX male is rare (1:20 000 in newborn males), and SRY positivity is responsible for this condition in approximately 90% of these subjects. External genitalia of 46,XX SRY-positive males appear as normal male external genitalia, and such cases are diagnosed when they present with small testes and/or infertility after puberty. Herein, we report an adolescent who presented with low testicular volume and who was diagnosed as a 46,XX male. SRY positivity was demonstrated in the patient by fluorescence in situ hybridization method. Conflict of interest:None declared.
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spelling pubmed-38902252014-01-22 46,XX Male Disorder of Sexual Development: A Case Report Anık, Ahmet Çatlı, Gönül Abacı, Ayhan Böber, Ece J Clin Res Pediatr Endocrinol Case Report The main factor influencing sex determination of an embryo is the sex-determining region Y (SRY), a master regulatory gene located on the Y chromosome. The presence of SRY causes the bipotential gonad to differentiate into a testis. However, some individuals carry a Y chromosome but are phenotypically female (46,XY females) or have a female karyotype but are phenotypically male (46,XX males). 46, XX male is rare (1:20 000 in newborn males), and SRY positivity is responsible for this condition in approximately 90% of these subjects. External genitalia of 46,XX SRY-positive males appear as normal male external genitalia, and such cases are diagnosed when they present with small testes and/or infertility after puberty. Herein, we report an adolescent who presented with low testicular volume and who was diagnosed as a 46,XX male. SRY positivity was demonstrated in the patient by fluorescence in situ hybridization method. Conflict of interest:None declared. Galenos Publishing 2013-12 2013-12-10 /pmc/articles/PMC3890225/ /pubmed/24379036 http://dx.doi.org/10.4274/Jcrpe.1098 Text en © Journal of Clinical Research in Pediatric Endocrinology, Published by Galenos Publishing. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of 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
Anık, Ahmet
Çatlı, Gönül
Abacı, Ayhan
Böber, Ece
46,XX Male Disorder of Sexual Development: A Case Report
title 46,XX Male Disorder of Sexual Development: A Case Report
title_full 46,XX Male Disorder of Sexual Development: A Case Report
title_fullStr 46,XX Male Disorder of Sexual Development: A Case Report
title_full_unstemmed 46,XX Male Disorder of Sexual Development: A Case Report
title_short 46,XX Male Disorder of Sexual Development: A Case Report
title_sort 46,xx male disorder of sexual development: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890225/
https://www.ncbi.nlm.nih.gov/pubmed/24379036
http://dx.doi.org/10.4274/Jcrpe.1098
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