Fanconi anemia (FA) is a rare inherited condition that affects your bone marrow and many other parts of your body. Your bone marrow is the spongy tissue in the center of your bones that creates stem cells that become red and white blood cells and platelets. If you have Fanconi anemia, your bone marrow doesn’t create healthy blood cells and platelets. People with FA have an increased risk of developing blood disorders and some kinds of cancer. FA also causes physical abnormalities that can affect people’s organs and appearances. People with FA that’s caused blood disorders are living longer and with fewer medical issues because they’re able to have bone marrow transplants.
Common FA Symptoms
Fanconi anemia affects people in many different ways, starting with how our bodies develop during gestation. FA may cause different symptoms linked to many different conditions, including anemia, bone marrow failure syndrome (aplastic anemia), cancer and physical abnormalities. For example, someone with FA may be very short or have problems with their bone structure. Many people have FA but don’t have obvious signs or symptoms.
Anemia Symptoms
Anemia is a common sign of FA. Symptoms include:
Treatment for Fanconi Anemia
Typically, healthcare providers focus on treatments to manage blood disorders that FA causes, including:
Prevention
Fanconi anemia is an inherited disorder. That means you can’t reduce your risk of developing FA. That said, if you have a family history of FA, you may want genetic testing to find out if you’re carrying FA. Not everyone who carries FA develops medical conditions. Likewise, not all people who carry FA pass it on to their children. Genetic testing will help you to understand your situation.