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1000 Titel
  • Pubertal development in 46,XY patients with NR5A1 mutations
1000 Autor/in
  1. Mönig, Isabel |
  2. Hoppmann, Julia |
  3. Johannsen, Trine Holm |
  4. Juul, Anders |
  5. Werner, Ralf |
  6. Lünstedt, Ralf |
  7. Birnbaum, Wiebke |
  8. Marshall, Louise |
  9. Wünsch, Lutz |
  10. Hiort, Olaf |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-10-06
1000 Erschienen in
1000 Quellenangabe
  • 75(2):601-613
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s12020-021-02883-y |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8816419/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Purpose!#!Mutations in the NR5A1 gene, encoding the transcription factor Steroidogenic Factor-1, are associated with a highly variable genital phenotype in patients with 46,XY differences of sex development (DSD). Our objective was to analyse the pubertal development in 46,XY patients with NR5A1 mutations by the evaluation of longitudinal clinical and hormonal data at pubertal age.!##!Methods!#!We retrospectively studied a cohort of 10 46,XY patients with a verified NR5A1 mutation and describe clinical features including the external and internal genitalia, testicular volumes, Tanner stages and serum concentrations of LH, FSH, testosterone, AMH, and inhibin B during pubertal transition.!##!Results!#!Patients who first presented in early infancy due to ambiguous genitalia showed spontaneous virilization at pubertal age accompanied by a significant testosterone production despite the decreased gonadal volume. Patients with apparently female external genitalia at birth presented later in life at pubertal age either with signs of virilization and/or absence of female puberty. Testosterone levels were highly variable in this group. In all patients, gonadotropins were constantly in the upper reference range or elevated. Neither the extent of virilization at birth nor the presence of Müllerian structures reliably correlated with the degree of virilization during puberty.!##!Conclusion!#!Patients with NR5A1 mutations regardless of phenotype at birth may demonstrate considerable virilization at puberty. Therefore, it is important to consider sex assignment carefully and avoid irreversible procedures during infancy.
1000 Sacherschließung
lokal Steroidogenic Factor 1/genetics [MeSH]
lokal Female [MeSH]
lokal Mutation [MeSH]
lokal Humans [MeSH]
lokal Retrospective Studies [MeSH]
lokal Differences of sex development
lokal Original Article
lokal Pubertal development
lokal Puberty/genetics [MeSH]
lokal Disorder of Sex Development, 46,XY/genetics [MeSH]
lokal Sexual Development [MeSH]
lokal Virilization
lokal Phenotype [MeSH]
lokal NR5A1 mutation
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0001-5071-6419|https://orcid.org/0000-0003-1436-1707|https://orcid.org/0000-0002-3303-5352|https://orcid.org/0000-0002-0534-4350|https://orcid.org/0000-0003-3718-3595|https://frl.publisso.de/adhoc/uri/TMO8bnN0ZWR0LCBSYWxm|https://frl.publisso.de/adhoc/uri/QmlybmJhdW0sIFdpZWJrZQ==|https://frl.publisso.de/adhoc/uri/TWFyc2hhbGwsIExvdWlzZQ==|https://frl.publisso.de/adhoc/uri/V8O8bnNjaCwgTHV0eg==|https://orcid.org/0000-0001-7490-4983
1000 Hinweis
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1000 Dateien
  1. Pubertal development in 46,XY patients with NR5A1 mutations
1000 Objektart article
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1000 @id frl:6444294.rdf
1000 Erstellt am 2023-04-27T12:42:04.647+0200
1000 Erstellt von 322
1000 beschreibt frl:6444294
1000 Zuletzt bearbeitet 2023-10-20T12:21:11.296+0200
1000 Objekt bearb. Fri Oct 20 12:21:11 CEST 2023
1000 Vgl. frl:6444294
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