What is Fanconi Anemia ?

This is an autosomal recessive condition, affected children usually develop severe aplastic anemia by age 8 to 9 years. Treatment usually consists of bone marrow transplant. Fanconi Anemia is not a cancer, though recent research has shown an association between Fanconi Anemia and leukemia. There are 8 types of Fanconi Anemia; known as complementation groups A through to H.

More About What is Fanconi Anemia ?

Fanconi Anemia is a rare disorder found in children that involves the blood and bone marrow. The symptoms include severe aplastic anemia, hypoplasia of the bone marrow, and patchy discoloration of the skin.

GIVE WITH CONFIDENCE

With Children’s Cancer Aid & Research Institute, your donation is used wisely to help children around the world.

We use industry standard communication protocols to ensure your personal information is encrypted and transmitted without risk.

Trusted Charity Since 1982

Your Impact in your inbox

See How You Can Make An Impact on Childhood Cancer!

Get Your Guide To Help End Childhood Cancer