XX testicular disorder of sex differentiation: case report

Detalhes bibliográficos
Autor(a) principal: Bianco,Bianca
Data de Publicação: 2011
Outros Autores: Christofolini,Denise Maria, Ghersel,Frederico Rezende, Gava,Marcello Machado, Barbosa,Caio Parente
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Einstein (São Paulo)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082011000300394
Resumo: ABSTRACT The 46 XX, testicular sex differentiation disorder, or XX male syndrome, is a rare condition detected by cytogenetics, in which testicular development occurs in the absence of the Y chromosome. It occurs in 1:20,000 to 25,000 male newborns and represents 2% of cases of male infertility. About 90% of individuals present with normal phenotype at birth and are generally diagnosed after puberty for hypoganadism, gynecomastia, and/or infertility. The authors present the report of an XX male with complete masculinization and infertility.
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spelling XX testicular disorder of sex differentiation: case reportGonadal dysgenesis, 46, XXGene, SRYSex differentiationinfertility, maleAzoospermiaCase reportsABSTRACT The 46 XX, testicular sex differentiation disorder, or XX male syndrome, is a rare condition detected by cytogenetics, in which testicular development occurs in the absence of the Y chromosome. It occurs in 1:20,000 to 25,000 male newborns and represents 2% of cases of male infertility. About 90% of individuals present with normal phenotype at birth and are generally diagnosed after puberty for hypoganadism, gynecomastia, and/or infertility. The authors present the report of an XX male with complete masculinization and infertility.Instituto Israelita de Ensino e Pesquisa Albert Einstein2011-09-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082011000300394einstein (São Paulo) v.9 n.3 2011reponame:Einstein (São Paulo)instname:Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)instacron:IIEPAE10.1590/s1679-45082011rc1862info:eu-repo/semantics/openAccessBianco,BiancaChristofolini,Denise MariaGhersel,Frederico RezendeGava,Marcello MachadoBarbosa,Caio Parenteeng2017-03-10T00:00:00Zoai:scielo:S1679-45082011000300394Revistahttps://journal.einstein.br/pt-br/ONGhttps://old.scielo.br/oai/scielo-oai.php||revista@einstein.br2317-63851679-4508opendoar:2017-03-10T00:00Einstein (São Paulo) - Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)false
dc.title.none.fl_str_mv XX testicular disorder of sex differentiation: case report
title XX testicular disorder of sex differentiation: case report
spellingShingle XX testicular disorder of sex differentiation: case report
Bianco,Bianca
Gonadal dysgenesis, 46, XX
Gene, SRY
Sex differentiation
infertility, male
Azoospermia
Case reports
title_short XX testicular disorder of sex differentiation: case report
title_full XX testicular disorder of sex differentiation: case report
title_fullStr XX testicular disorder of sex differentiation: case report
title_full_unstemmed XX testicular disorder of sex differentiation: case report
title_sort XX testicular disorder of sex differentiation: case report
author Bianco,Bianca
author_facet Bianco,Bianca
Christofolini,Denise Maria
Ghersel,Frederico Rezende
Gava,Marcello Machado
Barbosa,Caio Parente
author_role author
author2 Christofolini,Denise Maria
Ghersel,Frederico Rezende
Gava,Marcello Machado
Barbosa,Caio Parente
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Bianco,Bianca
Christofolini,Denise Maria
Ghersel,Frederico Rezende
Gava,Marcello Machado
Barbosa,Caio Parente
dc.subject.por.fl_str_mv Gonadal dysgenesis, 46, XX
Gene, SRY
Sex differentiation
infertility, male
Azoospermia
Case reports
topic Gonadal dysgenesis, 46, XX
Gene, SRY
Sex differentiation
infertility, male
Azoospermia
Case reports
description ABSTRACT The 46 XX, testicular sex differentiation disorder, or XX male syndrome, is a rare condition detected by cytogenetics, in which testicular development occurs in the absence of the Y chromosome. It occurs in 1:20,000 to 25,000 male newborns and represents 2% of cases of male infertility. About 90% of individuals present with normal phenotype at birth and are generally diagnosed after puberty for hypoganadism, gynecomastia, and/or infertility. The authors present the report of an XX male with complete masculinization and infertility.
publishDate 2011
dc.date.none.fl_str_mv 2011-09-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format report
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082011000300394
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082011000300394
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/s1679-45082011rc1862
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Instituto Israelita de Ensino e Pesquisa Albert Einstein
publisher.none.fl_str_mv Instituto Israelita de Ensino e Pesquisa Albert Einstein
dc.source.none.fl_str_mv einstein (São Paulo) v.9 n.3 2011
reponame:Einstein (São Paulo)
instname:Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
instacron:IIEPAE
instname_str Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
instacron_str IIEPAE
institution IIEPAE
reponame_str Einstein (São Paulo)
collection Einstein (São Paulo)
repository.name.fl_str_mv Einstein (São Paulo) - Instituto Israelita de Ensino e Pesquisa Albert Einstein (IIEPAE)
repository.mail.fl_str_mv ||revista@einstein.br
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