Check with your healthcare team for resources in your area. Because Kallmann Syndrome is rare, it may be difficult to find support groups in your area. There are support groups available for people with hypogonadotropic hypogonadism (HH) in general. There is a list of Yahoo and Facebook groups at the European GNRH Network site.
Other Questions About Kallman syndrome/hypogonadotropic hypogonadism
- Would a pituitary gland replacement be a cure for Kallman syndrome?
- Why does Kallmann Syndrome affect more males than females?
- Why can people with Kallmann Syndrome have reduced bone density?
- Who else in my family should I test for Kallmann Syndrome?
- Where do I find other people with Kallmann Syndrome ?
