Fanconi Anemia Research Fund
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Scan day: 13 February 2014 UTC
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Description: To find effective treatments and a cure for this disease, and to provide education and support services to affected families worldwide.
Home | Fanconi Anemia Research Fund Fanconi anemia (FA), named for Swiss pediatrician, Guido Fanconi, is a very rare, primarily recessive genetic disorder. If both parents carry a defect (mutation) in the same FA gene, each of their children has a 25% chance of inheriting the defective gene from both parents. When this happens, the child will have FA.
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| Page title: | Home | Fanconi Anemia Research Fund |
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| IP-address: | 198.101.244.50 |