What is Fanconi Anemia?
Fanconi Anemia (FA) is a rare, inherited blood disorder that leads to bone marrow failure. FA is a blood disorder, but it also can affect many other organs, tissues, and systems. Children who inherit FA are at higher risk of being born with birth defects. People who have FA are at higher risk of some cancers and other serious health problems.What are the signs and symptoms of Fanconi Anemia?
Physical findings can include the following:- Café au lait spots (brown birth marks)
- Short stature
- Abnormal thumbs, often including abnormal radii (these are the bones in the lower arm, between the elbow and the wrist)
- Abnormal male development
- Small head
- Small eyes
- Abnormal kidneys
How is Fanconi Anemia diagnosed?
- Physical examination for associated abnormalities.
- Blood tests including the chromosome breakage test and genetic testing or mutation analysis for genetic errors linked to FA.
- Bone Marrow evaluation.