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Pure gonadal dysgenesis (46 XX type) with a familial pattern
46, XX gonadal dysgenesis without the phenotype of Turner's syndrome is described as “pure”. Although, previous investigations obtained that commonly gonadal dysgenesis did not cause breast development as a result of low levels of circulating estradiol. However, in this study, we aimed to repor...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581097/ https://www.ncbi.nlm.nih.gov/pubmed/26430655 http://dx.doi.org/10.4103/2277-9175.162536 |
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author | Kohmanaee, Shahin Dalili, Setila Rad, Afagh Hassanzadeh |
author_facet | Kohmanaee, Shahin Dalili, Setila Rad, Afagh Hassanzadeh |
author_sort | Kohmanaee, Shahin |
collection | PubMed |
description | 46, XX gonadal dysgenesis without the phenotype of Turner's syndrome is described as “pure”. Although, previous investigations obtained that commonly gonadal dysgenesis did not cause breast development as a result of low levels of circulating estradiol. However, in this study, we aimed to report a familial pure gonadal dysgenesis with and without normal secondary sexual characteristics. In this study, we reported three siblings with pure gonadal dysgenesis with and without normal secondary sexual characteristics. The elder two sisters had a normal female phenotype and the youngest had amenorrhea with no breast development (B1) and pubic hair. In addition, it seems that the absence of pubic hair occurred due to delayed constitutional puberty. According to results, it seems that clinicians should consider different presentations for pure gonadal dysgenesis with familial pattern. |
format | Online Article Text |
id | pubmed-4581097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45810972015-10-01 Pure gonadal dysgenesis (46 XX type) with a familial pattern Kohmanaee, Shahin Dalili, Setila Rad, Afagh Hassanzadeh Adv Biomed Res Case Report 46, XX gonadal dysgenesis without the phenotype of Turner's syndrome is described as “pure”. Although, previous investigations obtained that commonly gonadal dysgenesis did not cause breast development as a result of low levels of circulating estradiol. However, in this study, we aimed to report a familial pure gonadal dysgenesis with and without normal secondary sexual characteristics. In this study, we reported three siblings with pure gonadal dysgenesis with and without normal secondary sexual characteristics. The elder two sisters had a normal female phenotype and the youngest had amenorrhea with no breast development (B1) and pubic hair. In addition, it seems that the absence of pubic hair occurred due to delayed constitutional puberty. According to results, it seems that clinicians should consider different presentations for pure gonadal dysgenesis with familial pattern. Medknow Publications & Media Pvt Ltd 2015-08-10 /pmc/articles/PMC4581097/ /pubmed/26430655 http://dx.doi.org/10.4103/2277-9175.162536 Text en Copyright: © 2015 Kohmanaee. http://creativecommons.org/licenses/by-nc-sa/3.0 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 author and source are credited. |
spellingShingle | Case Report Kohmanaee, Shahin Dalili, Setila Rad, Afagh Hassanzadeh Pure gonadal dysgenesis (46 XX type) with a familial pattern |
title | Pure gonadal dysgenesis (46 XX type) with a familial pattern |
title_full | Pure gonadal dysgenesis (46 XX type) with a familial pattern |
title_fullStr | Pure gonadal dysgenesis (46 XX type) with a familial pattern |
title_full_unstemmed | Pure gonadal dysgenesis (46 XX type) with a familial pattern |
title_short | Pure gonadal dysgenesis (46 XX type) with a familial pattern |
title_sort | pure gonadal dysgenesis (46 xx type) with a familial pattern |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581097/ https://www.ncbi.nlm.nih.gov/pubmed/26430655 http://dx.doi.org/10.4103/2277-9175.162536 |
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