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Hereditary elliptocytosis

Hereditary elliptocytosis is a disorder passed down through families in which the red blood cells are abnormally shaped.

See also:

Causes of Hereditary elliptocytosis

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.

Hereditary elliptocytosis Symptoms


  • Fatigue
  • Shortness of breath
  • Yellow skin and eyes (jaundice) - may continue for a long time in a newborn

Tests and Exams

An exam by your health care provider may show an enlarged spleen.

The following test results may help diagnose the condition:

  • Bilirubin level may be high.
  • Blood smear may show elliptical red blood cells.
  • Complete blood count (CBC) may show anemia or signs of red blood cell destruction.
  • Lactate dehydrogenase level may be high.
  • Ultrasound of the gallbladder may show gallstones.

Treatment of Hereditary elliptocytosis

There is no treatment needed for the disorder unless severe anemia or anemia symptoms occur. Surgery to remove the spleen may decrease the rate of red blood cell damage.

Prognosis (Outlook)

Most persons with hereditary elliptocytosis have no problems. They often do not know they have the condition.

Potential Complications

Elliptocytosis is often harmless. In mild cases, fewer than 15% of red blood cells are elliptical-shaped. However, some people may have crises in which the red blood cells rupture, especially if they have a viral infection. Persons with this disease can develop anemia, jaundice, and gallstones.

When to Contact a Health Professional

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 of Hereditary elliptocytosis

Genetic counseling may be appropriate for persons with a family history of this disease who wish to become parents.

References

Gallagher PG. Hemolytic anemias: red cell membrane and metabolic defects. In: Goldman L, Schafer AI, eds. Goldman's Cecil Medicine. 24th ed. Philadelphia, PA: Saunders Elsevier; 2011:chap 164.

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Review Date: 2/24/2014
Reviewed 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.
The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. © 1997- 2014 A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.
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