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2.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-213688

RESUMO

PURPOSE: To identify the clinical characteristics of SRY-negative male patients and genes related to male sex reversal, we performed a retrospective study using cases of 46,XX testicular disorders of sex development with a review of the literature. MATERIALS AND METHODS: SRY-negative cases of 46,XX testicular disorders of sex development referred for cytogenetic analysis from 1983 to 2013 were examined using clinical findings, seminal analyses, basal hormone profiles, conventional cytogenetic analysis and polymerase chain reaction. RESULTS: Chromosome analysis of cultured peripheral blood cells of 8,386 individuals found 19 cases (0.23%) with 46,XX testicular disorders of sex development. The SRY gene was confirmed to be absent in three of these 19 cases (15.8%). CONCLUSION: We report three rare cases of SRY-negative 46,XX testicular disorders of sex development. Genes on autosomes and the X chromosome that may have a role in sex determination were deduced through a literature review. These genes, through differences in gene dosage variation, may have a role in sex reversal in the absence of SRY.


Assuntos
Humanos , Masculino , Azoospermia , Células Sanguíneas , Análise Citogenética , Transtornos do Desenvolvimento Sexual , Dosagem de Genes , Genes sry , Infertilidade , Reação em Cadeia da Polimerase , Estudos Retrospectivos , Desenvolvimento Sexual , Cromossomo X
3.
Ann Pediatr Endocrinol Metab ; 20(4): 226-9, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26817010

RESUMO

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.

4.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-96136

RESUMO

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.


Assuntos
Feminino , Humanos , Masculino , Transtornos Cromossômicos , Transtornos do Desenvolvimento Sexual , Genes sry , Genitália , Disgenesia Gonadal Mista , Gônadas , Cariótipo , Programas de Rastreamento , Monossomia , Mosaicismo , Diferenciação Sexual , Síndrome de Turner
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