What is CHH/KS?

CHH: Short for Congenital Hypogonadotropic Hypogonadism, CHH is a condition that prevents puberty and causes infertility in both females and males.

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KS: In some people, the effects of CHH are combined with a lack of sense of smell. In those cases, the condition is called Kallmann syndrome. Both CHH and Kallmann syndrome are diagnosed and treated in the same way.

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What Causes CHH/KS?

CHH and KS are caused when there is not enough of the gonadotropin releasing hormone, also known as GnRH. 

Hormones are chemicals that carry messages from one part of the body to another. GnRH sends messages to the pituitary gland. When the pituitary gland receives a GnRH message, it releases two other hormones, luteinizing hormone (LH) and follicle stimulating hormone (FSH). LH and FSH are important for puberty and fertility in both females and males.

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In females

LH and FSH signal the ovaries to make estrogen and progesterone—hormones important for fertility.

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In males

LH and FSH signal the testes to make testosterone and sperm.

In people with CHH/KS, the lack of GnRH leads to low levels of LH and FSH. This leads to puberty disruption and infertility.
Recognize the Signs and Symptoms
Learn more about the underlying cause of CHH and KS

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