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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...

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Detalles Bibliográficos
Autores principales: Kohmanaee, Shahin, Dalili, Setila, Rad, Afagh Hassanzadeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
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.
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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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