Fanconi anemia is due to an abnormal gene that damages cells, which keeps them from repairing damaged DNA.

To inherit Fanconi anemia, a person must get one copy of the abnormal gene from each parent.

The condition is most often diagnosed in children between 3 and 14 years old.

People with Fanconi anemia have lower-than-normal numbers of white blood cells, red blood cells, and platelets (cells that help the blood clot).

Too few 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 anemia have some of these symptoms:

• Abnormal heart, lungs, and digestive tract
• Bone problems (especially the hips, spine or ribs) can cause a curved spine (scoliosis)
• Changes in the color of the skin, such as darkened areas of the skin, called café au lait spots, and vitiligo
• Deafness due to abnormal ears
• Eye or eyelid problems
• Kidneys that did not form correctly
• Problems with the arms and hands, such as missing, extra or misshapen thumbs, problems of the hands and the bone in the lower arm, and small or missing bone in the forearm
• Short height
• Small head
• Small testicles and genital changes

Other possible symptoms:

• Failure to thrive
• Learning disability
• Low birth weight
• Intellectual disability

Common tests for Fanconi anemia include:

• Bone marrow biopsy
• Complete blood count (CBC)
• Developmental tests
• Medicines added to a blood sample to check for damage to chromosomes
• Hand x-ray and other imaging studies (CT scan, MRI)
• Hearing test
• HLA tissue typing (to find matching bone-marrow donors)
• Ultrasound of the kidneys

Pregnant women may have amniocentesis or chorionic villous sampling to diagnose the condition in their unborn child.

People with mild to moderate blood cell changes who do not need a transfusion may only need regular check-ups and blood count checks. Their health care provider will closely monitor them for other cancers. These may include 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 anemia. (The best bone marrow donor is a brother or sister whose tissue type matches the person affected by Fanconi anemia.)

People 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 people respond to hormone therapy. But everyone with the disorder will quickly get worse when the medicines are stopped. In most cases, these medicines eventually stop working.

Additional treatments may include:

• Antibiotics (possibly given through a vein) to treat infections
• Blood transfusions to treat symptoms due to low blood counts
• Human papilloma virus and other vaccines

Most people with this condition visit a doctor on regular basis, specializing in treating:

• Blood disorders (hematologist)
• Diseases related to glands (endocrinologist)
• Eye diseases (ophthalmologist)
• Bone diseases (orthopedist)
• Kidney disease (nephrologist)
• Diseases related to female reproductive organs and breasts (gynecologist)

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.

People with Fanconi anemia are more likely to develop several types of blood disorders and cancers. These may include leukemia, myelodysplastic syndrome, and cancer of the head, neck, or urinary system.

Women with Fanconi anemia who become pregnant should be watched carefully by a specialist. Such women often need transfusions throughout pregnancy.

Men with Fanconi anemia have decreased fertility.

Complications of Fanconi anemia may include:

• Bone marrow failure
• Blood cancer
• Liver cancers (both benign and malignant)

Families with a history of this condition can have genetic counseling to better understand their risk.

Vaccination can reduce certain complications, including pneumococcal pneumonia, hepatitis, and varicella infections.

People with Fanconi anemia should avoid cancer-causing substances (carcinogens) and have regular check-ups to screen for cancer.

Fanconi's anemia; Anemia - Fanconi's

Dror Y. Inherited bone marrow failure syndromes. In: Hoffman R, Benz EJ, Silberstein LE, et al, eds. Hematology: Basic Principles and Practice. 8th ed. Philadelphia, PA: Elsevier; 2023:chap 30.

Lissauer T, Carroll W. Haematological disorders. In: Lissauer T, Carroll W, eds. Illustrated Textbook of Paediatrics. 6th ed. Philadelphia, PA: Elsevier; 2022:chap 23.

Vlachos A, Nash M, Lipton JM. Bone marrow failure. In: Fish JD, Lipton JM, Lanzkowsky P eds. Lanzkowsky's Manual of Pediatric Hematology and Oncology. 7th ed. Cambridge, MA: Elsevier Academic Press; 2022:chap 6.

Updated by: Todd Gersten, MD, Hematology/Oncology, Florida Cancer Specialists & Research Institute, Wellington, FL. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.