Prevalence of olfactory and other developmental anomalies in patients with central hypogonadotropic hypogonadism

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

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Bibliografiske detaljer

Principais autores:	Elisa eDella Valle, Silvia eVezzani, Vincenzo eRochira, Antonio Raffaele Michele Granata, Bruno eMadeo, Elisabetta eGenovese, Elisa ePignatti, Marco eMarino, Cesare eCarani, Manuela eSimoni
Format:	Artigo
Sprog:	Inglês
Udgivet:	Frontiers Media S.A. 2013-06-01
Serier:	Frontiers in Endocrinology
Fag:	Kallmann Syndrome Smell test developmental anomalies central hypogonadotropic hypogonadism hypothalamic-pituitary-gonadal axis neurosensorial hearing loss
Online adgang:	http://journal.frontiersin.org/Journal/10.3389/fendo.2013.00070/full
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