Prevalence of Olfactory and Other Developmental Anomalies in Patients with Central Hypogonadotropic Hypogonadism

Introduction: Hypogonadotropic hypogonadism (HH) is a heterogeneous disease caused by mutations in several genes. Based on the presence of hyposmia/anosmia it is distinguished into Kallmann syndrome (KS) and isolated HH. The prevalence of other developmental anomalies is not well established. Method...

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Detalhes bibliográficos
Main Authors: Della Valle, Elisa, Vezzani, Silvia, Rochira, Vincenzo, Granata, Antonio Raffaele Michele, Madeo, Bruno, Genovese, Elisabetta, Pignatti, Elisa, Marino, Marco, Carani, Cesare, Simoni, Manuela
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2013
Assuntos:
Endocrinology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3675377/
https://ncbi.nlm.nih.gov/pubmed/23760293
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2013.00070
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