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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Detalles Bibliográficos
Autores principales: Della Valle, Elisa, Vezzani, Silvia, Rochira, Vincenzo, Granata, Antonio Raffaele Michele, Madeo, Bruno, Genovese, Elisabetta, Pignatti, Elisa, Marino, Marco, Carani, Cesare, Simoni, Manuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675377/
https://www.ncbi.nlm.nih.gov/pubmed/23760293
http://dx.doi.org/10.3389/fendo.2013.00070

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675377/
https://www.ncbi.nlm.nih.gov/pubmed/23760293
http://dx.doi.org/10.3389/fendo.2013.00070

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