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Information on this site is provided by people with personal experience of Kallmann's syndrome. Symptoms and appropriate treatments are different for different people. You should not treat anything on this site as a substitute for advice from a trained medical professional.
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- Site Counter: 651563Unique Visitor: 100844Registered Users: 3732Unregistered Users: 231Published Nodes: 719Unpublished Nodes: 0Your IP: 38.107.179.240Since: 2008-06-29
© 2008 Neil Smith
Brother with KS
16 August 2010 - 1:33am — angie101
My brother has KS and I'm trying to determine if it is a sporadic case or genetic. There's no family history, but my dad has no sense of smell. Is this just a coincidence or is it indicative of something hereditary? My husband and I plan on starting a family soon and are wondering if I am a carrier of KS. My brother will need to know his odds of passing it on at some point too.

