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Hereditary elliptocytosis is a disorder passed down through families in which the red blood cells are oval-shaped.
See also: Hereditary spherocytosis
Elliptocytosis affects about 1 in every 2,500 people of northern European heritage. It is more common in people of African and Mediterranean descent. You are more likely to develop this condition if someone in your family has had it.
An examination by your health care provider may occasionally show an enlarged spleen.
The following tests may help diagnose the condition:
There is no treatment needed for the disorder unless red blood cells rupture. Surgery to remove the spleen may decrease red blood cell rupture.
Most persons with hereditary elliptocytosis have no problems, and are unaware of their condition.
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.
Call for an appointment with your health care provider if you have jaundice that doesn't go away or symptoms of anemia or gallstones.
Genetic counseling may be appropriate for persons with a family history of this disease who wish to become parents.
Elliptocytosis - hereditary
Golan DE. Hemolytic anemias: red cell membrane and metabolic defects. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 165.
Updated by: David C. Dugdale, III, MD, Professor of Medicine, Division of General Medicine, Department of Medicine, University of Washington School of Medicine; and James R. Mason, MD, Oncologist, Director, Blood and Marrow Transplantation Program and Stem Cell Processing Lab, Scripps Clinic, Torrey Pines, California. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.
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Page last updated: 29 October 2009 |