Who else in the family should be tested for Kallmann syndrome depends on the mode of inheritance. For example, if the gene is inherited in an x-linked manner, other males in the family should be tested. This can include brothers of an affected male and sons of an affected female. If the gene is autosomal recessive, it may be necessary to test siblings of an affected person. Parents of the affected person may also wish to be tested so that they may inform their siblings of carrier status. If the gene is autosomal dominant, it may be recommended to test parents, siblings, children, aunts and uncles. Check with your doctor or genetic counselor for more information about who should be tested based on the mode of inheritance.
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 ?
