References in periodicals archive ?
Inactivating KISS1 mutation and hypogonadotropic hypogonadism," The New England Journal of Medicine, vol.
The report provides a snapshot of the global therapeutic landscape of Hypogonadotropic Hypogonadism
Partial hypogonadotropic hypogonadism associated with the Leu266Arg and Gln106Arg mutation of the gonadotropin-releasing hormone receptor.
Hypogonadotropic hypogonadism (HH) is a leading cause of pubertal delay, which is characterized by failure of initiation of puberty due to insufficient gonadotropin and sex steroids release which results in failure of development of secondary sexual characteristics and maturation of reproductive system (Seminara et al.
Induction of fertility in a man with hypogonadotropic hypogonadism with very low seminal volume.
Mutation and targeted deletion of KISS1 as well as KISS1R result in the hypogonadotropic hypogonadism in human and rodents (de Roux et al.
Congenital hypogonadotropic hypo-gonadism can be due to one of several gene defects13,14.
9,10) Treatment of hypogonadism in the male who wishes to maintain their fertility potential or as attempted treatment to improve abnormal semen parameters in men with hypogonadotropic hypogonadism includes the use of the selective estrogen receptor modulator Clomiphene citrate and human Chorionic Gonadotropin (hCG) which has an LH effect on the testes.
Congenital hypogonadotropic hypogonadism and micropenis: effect of testosterone treatment on adult penile size--why sex reversal is not indicated.
Moebius-Poland syndrome and hypogonadotropic hypogonadism.