Hypogonadotropic Hypogonadism with Cushing?s Disease-A Case Report

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Behçet Syndrome and Hypogonadotropic Hypogonadism: case report

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Hypogonadotropic hypogonadism presenting with arhinia: a case report

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I-3: Hypogonadotropic Hypogonadism

Hypogonadotropic hypogonadism (HH) is an uncommon cause of male infertility and a congenital or secondary disorder characterized by delayed or absent sexual maturation. Congenital abnormalities leading to HH are usually the consequence of deficient GnRH secretion occurring either in isolation (idiopathic hypogonadotropic hypogonadism (IHH)), or in association with anosmia (Kallmann syndrome; KS...

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MANAGEMENT OF ENDOCRINE DISEASE: Reversible hypogonadotropic hypogonadism.

Congenital hypogonadotropic hypogonadism (CHH) is characterized by lack of puberty and infertility. Traditionally, it has been considered a life-long condition yet cases of reversibility have been described wherein patients spontaneously recover function of the reproductive axis following treatment. Reversibility occurs in both male and female CHH cases and appears to be more common (~10-15%) t...

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ژورنال

عنوان ژورنال: Clinics in Mother and Child Health

سال: 2015

ISSN: 2090-7214

DOI: 10.4172/2090-7214.1000179