Congenital hypogonadotropic hypogonadism (CHH) is a rare genetic condition of central hypogonadism that results in absent or incomplete pubertal development and reproductive immaturity. It has an estimated incidence of between 1 in 15,000 and 1 in 50,000, and a male-to-female predominance of 3.6 to one.

Male congenital hypogonadotropic hypogonadism (CHH) is a heterogenous group of genetic disorders that cause impairment in the production or action of gonadotropin releasing hormone (GnRH). These defects result in dysfunction of the ...

Congenital hypogonadotropic hypogonadism (CHH) is a form of HH that occurs in ~1 in 4000 births. It is a relatively rare heterogeneous disorder caused by deficient production, secretion, or action of gonadotropin-releasing hormone (GnRH).

Objective: Congenital hypogonadotropic hypogonadism (CHH) and constitutional delay of growth and puberty (CDGP) represent rare and common forms of GnRH deficiency, respectively. Both CDGP and CHH present with delayed puberty, and the distinction between these two entities during early adolescence is challenging.

Congenital hypogonadotropic hypogonadism (CHH) is a rare endocrine disorder that results in reproductive hormone deficiency and reduced potential for fertility in adult life.

Mar 28, 2020 · Congenital hypogonadotropic hypogonadism (CHH) is a genetic condition characterized by incomplete or absent puberty and infertility due to central (tertiary or hypothalamic) hypogonadism caused by gonadotropic …

Apr 1, 2019 · Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder that results from the failure of the normal episodic GnRH secretion, leading to delayed puberty and infertility. CHH can be associated with an absent sense of smell, also termed Kallmann syndrome, or with other anomalies.

Mar 28, 2019 · Congenital hypogonadotropic hypogonadism (CHH) is a rare genetic disorder caused by the absence of GnRH secretion from the hypothalamus or defective GnRH action in the pituitary. CHH patients present with absent or incomplete sexual maturation and infertility, with...

May 11, 2023 · Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder resulting from a deficient secretion of the episodic gonadotropin-releasing hormone, leading to delayed or absent puberty and infertility. In female patients with CHH, the most commonly used treatment is gonadotropin (Gn) therapy.

Key Points: Consonants are all the letters that aren't vowels. 'wh' is another consonant digraph that makes just one sound.