Fanconi's anemia is a disease passed down through families (inherited) that mainly affects the bone marrow. It results in decreased production of all types of blood cells.
Fanconi's anemia is different from Fanconi syndrome, a rare kidney disorder.
Fanconi's anemia is due to an abnormal gene that damages cells, which keeps them from repairing damaged DNA.
To inherit Fanconi's anemia, a person must get one copy of the abnormal gene from each parent.
The condition is usually diagnosed in children between 2 and 15 years old.
Persons with Fanconi's anemia have lower-than-normal numbers of white blood cells, red blood cells, and platelets (cells that help the blood clot).
Not enough white blood cells can lead to infections. A lack of red blood cells may result in fatigue (anemia).
A lower-than-normal amount of platelets may lead to excess bleeding.
Most people with Fanconi's anemia have some of these symptoms:
Other possible symptoms:
Common tests for Fanconi's anemia include:
Patients with mild to moderate blood cell changes who do not need a transfusion may only need regular check-ups and blood count checks. The health care provider will closely monitor the person for other cancers, usually leukemia or cancers of the head, neck, or urinary system.
Medicines called growth factors (such as erythropoietin, G-CSF, and GM-CSF) can improve blood counts for a short while.
A bone marrow transplant can cure the blood count problems of Fanconi's anemia. (The best donor is a brother or sister whose tissue type matches the patient.)
Persons who have had a successful bone marrow transplant still need regular check-ups because of the risk for additional cancers.
Hormone therapy combined with low doses of steroids (such as hydrocortisone or prednisone) is prescribed to those who do not have a bone marrow donor. Most patients respond to hormone therapy. But everyone with the disorder will quickly get worse when the drugs are stopped. In most cases, these drugs eventually stop working.
Additional treatments may include:
Most people with this condition visit a blood disorder specialist (hematologist), a doctor who treats diseases related to glands (endocrinologist), and an eye doctor (ophthalmologist) regularly. They also may see a bone doctor (orthopedist), gynecologist, or kidney disease specialist (nephrologist).
The survival rates vary from person to person. The outlook is poor in those with low blood counts. New and improved treatments, such as bone marrow transplants, have likely improved survival.
Persons with Fanconi's anemia are more likely to develop several types of blood disorders and cancers, including leukemia, myelodysplastic syndrome, and cancer of the head, neck, or urinary system.
Women with Fanconi's anemia who become pregnant should be watched carefully by a doctor. Such women often need transfusions throughout pregnancy.
Men with Fanconi's anemia have decreased fertility.
Families with this condition can have genetic counseling to better understand their risk.
Vaccination can reduce certain complications, including pneumococcal pneumonia, hepatitis, and varicella infections.
Persons with Fanconi's anemia should avoid cancer-causing substances (carcinogens) and have regular check-ups to screen for cancer.
Anemia - Fanconi's
Castro-Malaspina H, O’Reilly RJ. Aplastic anemia and related disorders. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 171.
Bagby GC. Aplastic anemia and related bone marrow failure states. In: Goldman L, Schafer AI, eds. Cecil Medicine. 24th ed. Philadelphia, Pa: Saunders Elsevier; 2011:chap 168.
Updated by: Todd Gersten, MD, Hematology/Oncology, Florida Cancer Specialists & Research Institute, Wellington, FL. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team.
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