Fanconi's anemia

Injury	Disease	Nutrition	Poison

Symptoms	Surgery	Test	Special Topic

Formed elements of blood

Overview

Symptoms

Treatment

Prevention

Fanconi's anemia

Definition:

Fanconi's anemia is an inherited disease that primarily affects the bone marrow, resulting in decreased production of all types of blood cells. The lack of white blood cells predisposes the patient to infections, while the lack of platelets and red blood cells may result in bleeding, and fatigue (anemia), respectively. It is also associated with a broad variety of physical anomalies.

Fanconi's anemia is distinct from Fanconi's syndrome, a rare kidney disorder in which nutrients are lost through the urine.

Alternative Names:

Anemia - Fanconi's; FA

Causes, incidence, and risk factors:

Fanconi's anemia is inherited in an autosomal recessive fashion, thus one copy of an abnormal gene is passed on by each parent. It occurs in all racial and ethnic groups. It is classically diagnosed between 2 and 15 years of age.

The disease is caused by a genetic defect that prevents cells from fixing damaged DNA or removing toxic, oxygen free radicals that damage cells. Patients may be suspected of having the disease if they have particular birth defects or develop decreased blood counts.

Review Date: 7/29/2005
Reviewed By: William Matsui, M.D., Assistant Professor of Oncology, Division of Hematologic Malignancies, The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD. Review provided by VeriMed Healthcare Network.

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