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Frontiers Media, Frontiers in Endocrinology, (4)
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Prevalence of Olfactory and Other Developmental Anomalies in Patients with Central Hypogonadotropic Hypogonadism
Journal article published in 2013 by
Elisa Della Valle,
Silvia Vezzani,
Vincenzo Rochira 
,
Antonio Raffaele Michele Granata,
Bruno Madeo,
Elisabetta Genovese,
Elisa Pignatti,
Marco Marino,
Cesare Carani,
Manuela Simoni
,
Antonio Raffaele Michele Granata,
Bruno Madeo,
Elisabetta Genovese,
Elisa Pignatti,
Marco Marino,
Cesare Carani,
Manuela Simoni
This paper is made freely available by the publisher.
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Abstract
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.