Fanconi anemia - Wikipedia, the free encyclopedia
Fanconi anemia (FA) is a genetic disease that affects children and adults from all ethnic backgrounds. It is rare, with an overall incidence of 1 per 350000 ...
http://en.wikipedia.org/wiki/Fanconi_anemia...
|
What is Fanconi anemia (FA)?
Fanconi anemia, or FA, is a rare, inherited blood disorder that leads to bone marrow failure.
http://www.nhlbi.nih.gov/health/dci/Diseases/fanconi/fanconi...
|
Fanconi's anemia: MedlinePlus Medical Encyclopedia
18 Dec 2009 ... Fanconi's anemia is disease passed down through families (inherited) that mainly affects the bone marrow. It results in decreased production ...
http://www.nlm.nih.gov/medlineplus/ency/article/000334.htm...
|
OMIM - FANCONI ANEMIA; FA
Fanconi ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650...
|
Fanconi anemia (FA) treatment
Doctors decide how to treat Fanconi anemia (FA) based on a person's age and how well (or how poorly) the person's bone marrow is making new blood cells.
http://www.nhlbi.nih.gov/health/dci/Diseases/fanconi/fanconi...
|
The Rockefeller University - Fanconi Anemia Mutation Database
The Fanconi Anemia Mutation Database was established in 1998 as a cooperative effort to accelerate the availability of information on mutations in these ...
http://www.rockefeller.edu/fanconi/mutate/...
|
Fanconi anemia diagnosis, genetic testing
People who have Fanconi anemia (FA) are born with the disorder.
http://www.nhlbi.nih.gov/health/dci/Diseases/fanconi/fanconi...
|
Fanconi Anemia -- GeneReviews -- NCBI Bookshelf
Fanconi anemia (FA) is the most common genetic cause of aplastic anemia and one of the most common genetic causes of hematologic malignancy. ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part...
|
Fanconi anemia symptoms
Your doctor may suspect you or your child has Fanconi anemia (FA) if you have signs and symptoms of anemia, bone marrow failure, birth defects, ...
http://www.nhlbi.nih.gov/health/dci/Diseases/fanconi/fanconi...
|
Fanconi anemia.
Fanconi anemia (FA) is a rare hereditary disease characterized by bone marrow failure and developmental anomalies; a high incidence of myelodysplasia (MDS), ...
http://www.ncbi.nlm.nih.gov/pubmed/16822457...
|