hypogonadism

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Related to hypogonadotropic hypogonadism: hypergonadotropic hypogonadism, primary hypogonadism

hypogonadism

[‚hī·pō′gō‚na‚diz·əm]
(medicine)
Reduced hormonal secretion by the testes or ovaries.
References in periodicals archive ?
Outcome of gonadotropin therapy for male hypogonadotropic hypogonadism at university affiliated male infertility centers: a 30-year retrospective study.
A novel mutation in DAX1 causes delayed-onset adrenal insufficiency and incomplete hypogonadotropic hypogonadism," The Journal of Clinical Investigation, vol.
Predictive value of luteinizing hormone releasing hormone (LHRH) bolus testing before and after 36-hour pulsatile LHRH administration in the differential diagnosis of constitutional delay of puberty and male hypogonadotropic hypogonadism.
Predictors of outcome of long-term GnRH therapy in men with idiopathic hypogonadotropic hypogonadism.
Three (2 females and 1 males) out of our 4 hypogonadal patients had hypergonadotropic hypogonadism, and 1 female patient had hypogonadotropic hypogonadism.
Partial hypogonadotropic hypogonadism associated with the Leu266Arg and Gln106Arg mutation of the gonadotropin-releasing hormone receptor.
In Chapter 10, the authors review the genetics of neurokinin B and its receptor and their role in the regulation of human GnRH secretion in hypogonadotropic hypogonadism (HH).
For males, Gonal-f(R) has been approved in 56 countries worldwide for gonadal dysfunction associated with absence of sperm in the semen or male hypogonadotropic hypogonadism.
Key Words: anastrazole, aromatase, hypogonadism, idiopathic hypogonadotropic hypogonadism, premature ejaculation
A clear, colorless gel containing 1% testosterone for replacement therapy in men with primary or hypogonadotropic hypogonadism.
Post study analysis of the population studied in a recently completed Androxal[TM] trial was consistent with men who had Adult-Onset Idiopathic Hypogonadotropic Hypogonadism (AIHH).
The deficiency in release or action of GnRH leads to hypogonadotropic hypogonadism (HH) characterized by low FSH, LH and testosterone (T) and absent or impaired sexual development at puberty.