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Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene

Turner syndrome is the most common chromosomal disorder in girls. Various phenotypic features show depending upon karyotype from normal female through ambiguous genitalia to male. Usually, Turner girls containing 45,X/46,XY mosaicism, or sex-determining region Y (SRY) gene may have mixed gonadal dys...

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Autores principales: Jung, Jae Yeop, Yang, Sohyoung, Jeong, Eun-Hwan, Lee, Ho-Chang, Lee, Yong-Moon, Han, Heon-Seok, Yi, Kyung Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Endocrinology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4722163/
https://www.ncbi.nlm.nih.gov/pubmed/26817010
http://dx.doi.org/10.6065/apem.2015.20.4.226
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author Jung, Jae Yeop
Yang, Sohyoung
Jeong, Eun-Hwan
Lee, Ho-Chang
Lee, Yong-Moon
Han, Heon-Seok
Yi, Kyung Hee
author_facet Jung, Jae Yeop
Yang, Sohyoung
Jeong, Eun-Hwan
Lee, Ho-Chang
Lee, Yong-Moon
Han, Heon-Seok
Yi, Kyung Hee
author_sort Jung, Jae Yeop
collection PubMed
description Turner syndrome is the most common chromosomal disorder in girls. Various phenotypic features show depending upon karyotype from normal female through ambiguous genitalia to male. Usually, Turner girls containing 45,X/46,XY mosaicism, or sex-determining region Y (SRY) gene may have mixed gonadal dysgenesis with various external sexual differentiation. We experienced a short statured 45,X Turner girl with normal external genitalia. Because SRY gene was positive, laparoscopic gonadectomy was performed. The dysgenetic gonads revealed bilateral ovotesticular tissues. The authors report a mixed gonadal dysgenesis case found in clinical 45,X Turner patient with positive SRY gene. Screening for SRY gene should be done even the karyotype is 45,X monosomy and external genitalia is normal.
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spelling pubmed-47221632016-01-26 Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene Jung, Jae Yeop Yang, Sohyoung Jeong, Eun-Hwan Lee, Ho-Chang Lee, Yong-Moon Han, Heon-Seok Yi, Kyung Hee Ann Pediatr Endocrinol Metab Case Report Turner syndrome is the most common chromosomal disorder in girls. Various phenotypic features show depending upon karyotype from normal female through ambiguous genitalia to male. Usually, Turner girls containing 45,X/46,XY mosaicism, or sex-determining region Y (SRY) gene may have mixed gonadal dysgenesis with various external sexual differentiation. We experienced a short statured 45,X Turner girl with normal external genitalia. Because SRY gene was positive, laparoscopic gonadectomy was performed. The dysgenetic gonads revealed bilateral ovotesticular tissues. The authors report a mixed gonadal dysgenesis case found in clinical 45,X Turner patient with positive SRY gene. Screening for SRY gene should be done even the karyotype is 45,X monosomy and external genitalia is normal. The Korean Society of Pediatric Endocrinology 2015-12 2015-12-31 /pmc/articles/PMC4722163/ /pubmed/26817010 http://dx.doi.org/10.6065/apem.2015.20.4.226 Text en © 2015 Annals of Pediatric Endocrinology & Metabolism http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jung, Jae Yeop
Yang, Sohyoung
Jeong, Eun-Hwan
Lee, Ho-Chang
Lee, Yong-Moon
Han, Heon-Seok
Yi, Kyung Hee
Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene
title Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene
title_full Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene
title_fullStr Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene
title_full_unstemmed Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene
title_short Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene
title_sort mixed gonadal dysgenesis in 45,x turner syndrome with sry gene
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4722163/
https://www.ncbi.nlm.nih.gov/pubmed/26817010
http://dx.doi.org/10.6065/apem.2015.20.4.226
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