OR17-2 Comprehensive Genetic Investigation of Patients with Central Precocious Puberty Associated with Complex Phenotypes

Background: Idiopathic central precocious puberty (CPP) is mostly described as an isolated entity. A few studies have shown its association with clinical syndromes and rare cases of chromosomal abnormalities. Objective: To clinically characterize and to genetically investigate a cohort of patients w...

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Foilsithe in:J Endocr Soc
Main Authors: Canton, Ana, Brito, Vinicius, Montenegro, Luciana, Krepischi, Ana, Rosenberg, Carla, Costa, Silvia, Ramos, Carolina, Cunha, Marina, Seraphim, Carlos, Faria, Aline, Funari, Mariana, Jorge, Alexander, de Zegher, Francis, Mendonca, Berenice, Latronico, Ana Claudia
Formáid: Artigo
Teanga:Inglês
Foilsithe: Endocrine Society 2019
Ábhair:
Pediatric Endocrinology
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6555075/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-OR17-2
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