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Hereditary elliptocytosis Health Article
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Definition
Hereditary elliptocytosis is a disorder passed down through families in which the red blood cells are oval-shaped. See also: Hereditary spherocytosis
Alternative Names
Causes, incidence, and risk factors
Elliptocytosis affects about 1 in every 4,000-5,000 people. It is most common in people of African and Mediterranean descent. You are more likely to develop this condition if someone in your family has had it.
Symptoms
Signs and tests
An examination by your health care provider may occasionally show an enlarged spleen. The following tests may help diagnose the condition:
Treatment
There is no treatment needed for the disorder unless red blood cells rupture. Surgery to remove the spleen may decrease red blood cell rupture.
Expectations (prognosis)
Most persons with hereditary elliptocytosis have no problems, and are unaware of their condition.
Complications
Elliptocytosis is frequently harmless. In mild cases, fewer than 15% of red blood cells are oval-shaped. However, some people may have crises in which the red blood cells rupture, releasing their hemoglobin. Persons with this disease can develop anemia, jaundice, and gallstones.
Calling your health care provider
Call for an appointment with your health care provider if you have jaundice that doesn't go away or symptoms of anemia or gallstones.
Prevention
Genetic counseling may be appropriate for persons with a family history of this disease who wish to become parents.
References
Gallagher PG. Hereditary elliptocytosis: spectrin and protein 4.1R. Semin Hematol. 2004 Apr; 41(2): 142-64. Kasper D, Braunwald E, Fauci A, et al. Harrison's Principals of Internal Medicine. 16th edition [online version]. New York, NY: McGraw Hill; 2005. Hoffman R, Benz EJ, Shattil SS, et al. Hematology: Basic Principles and Practice. 4th ed. Orlando, Fl: Churchill Livingstone; 2005. |
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