Spontaneous puberty in girls with early diagnosis of Turner syndrome

Detalhes bibliográficos
Autor(a) principal: Carpini,Stela
Data de Publicação: 2012
Outros Autores: Carvalho,Annelise Barreto, Guerra-Júnior,Gil, Baptista,Maria Tereza Matias, Lemos-Marini,Sofia Helena Valente, Maciel-Guerra,Andréa Trevas
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Arquivos Brasileiros de Endocrinologia & Metabologia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302012000900009
Resumo: OBJECTIVE: To verify if the frequency of spontaneous pubertal development among girls with Turner syndrome (TS) diagnosed in infancy and childhood is greater than that of patients diagnosed later. SUBJECTS AND METHODS: Thirty three girls aged < 10 years at the time of diagnosis were evaluated regarding pubertal development. The frequency of spontaneous puberty was compared with that of girls aged &gt; 13 years diagnosed at the same service. RESULTS: Sixteen of 32 informative patients had signs of spontaneous puberty, a frequency greater than that of patients diagnosed later. In six patients, there was no progression of puberty; menarche occurred in six, and one became pregnant, but the fetus was a stillborn. Spontaneous puberty was absent in all cases with 45,X karyotype. CONCLUSIONS: The greater prevalence of spontaneous puberty in girls whose diagnosis was not based on pubertal delay suggests that, among those diagnosed later, there is a bias towards patients with hypogonadism. Arq Bras Endocrinol Metab. 2012;56(9):653-7
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spelling Spontaneous puberty in girls with early diagnosis of Turner syndromeTurner syndromeearly diagnosisgonadal dysgenesispubertyOBJECTIVE: To verify if the frequency of spontaneous pubertal development among girls with Turner syndrome (TS) diagnosed in infancy and childhood is greater than that of patients diagnosed later. SUBJECTS AND METHODS: Thirty three girls aged < 10 years at the time of diagnosis were evaluated regarding pubertal development. The frequency of spontaneous puberty was compared with that of girls aged &gt; 13 years diagnosed at the same service. RESULTS: Sixteen of 32 informative patients had signs of spontaneous puberty, a frequency greater than that of patients diagnosed later. In six patients, there was no progression of puberty; menarche occurred in six, and one became pregnant, but the fetus was a stillborn. Spontaneous puberty was absent in all cases with 45,X karyotype. CONCLUSIONS: The greater prevalence of spontaneous puberty in girls whose diagnosis was not based on pubertal delay suggests that, among those diagnosed later, there is a bias towards patients with hypogonadism. Arq Bras Endocrinol Metab. 2012;56(9):653-7Sociedade Brasileira de Endocrinologia e Metabologia2012-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302012000900009Arquivos Brasileiros de Endocrinologia &amp; Metabologia v.56 n.9 2012reponame:Arquivos Brasileiros de Endocrinologia & Metabologia (Online)instname:Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)instacron:SBEM10.1590/S0004-27302012000900009info:eu-repo/semantics/openAccessCarpini,StelaCarvalho,Annelise BarretoGuerra-Júnior,GilBaptista,Maria Tereza MatiasLemos-Marini,Sofia Helena ValenteMaciel-Guerra,Andréa Trevaseng2013-01-15T00:00:00Zoai:scielo:S0004-27302012000900009Revistahttps://www.aem-sbem.com/ONGhttps://old.scielo.br/oai/scielo-oai.php||abem-editoria@endocrino.org.br1677-94870004-2730opendoar:2013-01-15T00:00Arquivos Brasileiros de Endocrinologia & Metabologia (Online) - Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)false
dc.title.none.fl_str_mv Spontaneous puberty in girls with early diagnosis of Turner syndrome
title Spontaneous puberty in girls with early diagnosis of Turner syndrome
spellingShingle Spontaneous puberty in girls with early diagnosis of Turner syndrome
Carpini,Stela
Turner syndrome
early diagnosis
gonadal dysgenesis
puberty
title_short Spontaneous puberty in girls with early diagnosis of Turner syndrome
title_full Spontaneous puberty in girls with early diagnosis of Turner syndrome
title_fullStr Spontaneous puberty in girls with early diagnosis of Turner syndrome
title_full_unstemmed Spontaneous puberty in girls with early diagnosis of Turner syndrome
title_sort Spontaneous puberty in girls with early diagnosis of Turner syndrome
author Carpini,Stela
author_facet Carpini,Stela
Carvalho,Annelise Barreto
Guerra-Júnior,Gil
Baptista,Maria Tereza Matias
Lemos-Marini,Sofia Helena Valente
Maciel-Guerra,Andréa Trevas
author_role author
author2 Carvalho,Annelise Barreto
Guerra-Júnior,Gil
Baptista,Maria Tereza Matias
Lemos-Marini,Sofia Helena Valente
Maciel-Guerra,Andréa Trevas
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Carpini,Stela
Carvalho,Annelise Barreto
Guerra-Júnior,Gil
Baptista,Maria Tereza Matias
Lemos-Marini,Sofia Helena Valente
Maciel-Guerra,Andréa Trevas
dc.subject.por.fl_str_mv Turner syndrome
early diagnosis
gonadal dysgenesis
puberty
topic Turner syndrome
early diagnosis
gonadal dysgenesis
puberty
description OBJECTIVE: To verify if the frequency of spontaneous pubertal development among girls with Turner syndrome (TS) diagnosed in infancy and childhood is greater than that of patients diagnosed later. SUBJECTS AND METHODS: Thirty three girls aged < 10 years at the time of diagnosis were evaluated regarding pubertal development. The frequency of spontaneous puberty was compared with that of girls aged &gt; 13 years diagnosed at the same service. RESULTS: Sixteen of 32 informative patients had signs of spontaneous puberty, a frequency greater than that of patients diagnosed later. In six patients, there was no progression of puberty; menarche occurred in six, and one became pregnant, but the fetus was a stillborn. Spontaneous puberty was absent in all cases with 45,X karyotype. CONCLUSIONS: The greater prevalence of spontaneous puberty in girls whose diagnosis was not based on pubertal delay suggests that, among those diagnosed later, there is a bias towards patients with hypogonadism. Arq Bras Endocrinol Metab. 2012;56(9):653-7
publishDate 2012
dc.date.none.fl_str_mv 2012-12-01
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302012000900009
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0004-27302012000900009
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Endocrinologia e Metabologia
publisher.none.fl_str_mv Sociedade Brasileira de Endocrinologia e Metabologia
dc.source.none.fl_str_mv Arquivos Brasileiros de Endocrinologia &amp; Metabologia v.56 n.9 2012
reponame:Arquivos Brasileiros de Endocrinologia & Metabologia (Online)
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