Idiopathic central precocious puberty in a Klinefelter patient: highlights on gonadotropin levels and pathophysiology

BACKGROUND: Idiopathic central precocious puberty (ICPP) is supposed to be non-existent in a context of testicular destruction that is typically present in Klinefelter syndrome (KS). Herein, we describe a rare case of ICPP in a Klinefelter patient (47,XXY) with 2 maternal X chromosomes. Moreover, we...

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Dettagli Bibliografici
Pubblicato in:Basic Clin Androl
Autori principali: Maqdasy, Salwan, Barres, Bertrand, Salaun, Gaelle, Batisse-Lignier, Marie, Pebrel-Richard, Celine, Kwok, Kelvin H. M., Labbé, André, Touraine, Philippe, Brugnon, Florence, Tauveron, Igor
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2020
Soggetti:
Case Report
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7724694/
https://ncbi.nlm.nih.gov/pubmed/33292161
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12610-020-00117-1
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