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Who Is Affected by Sickle Cell Disease

Sickle cell disease is an inherited disorder. More specifically, sickle cell disease is an autosomal recessive disease. This means that to have the disease, a person must inherit an abnormal gene from both parents.

People whose ancestors were from Africa, India, the Middle East, the Mediterranean (Turkey, Italy, Greece), and some Latin American countries are more likely to inherit the gene that can cause sickle cell disease. In the United States, about 2,000 children are born each year with sickle cell disease.1

Recommended Related to Blood Disorders

Sickle Cell Disease

Important It is possible that the main title of the report Sickle Cell Disease is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.

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Some people inherit one sickle cell gene and one other defective hemoglobin gene. This results in similar sickle cell disorders ranging from mild to severe.

Citations

  1. Wang WC (2009). Sickle cell anemia and other sickling syndromes. In JP Greer et al., eds., Wintrobe's Clinical Hematology, 12th ed., pp. 1038-1082. Philadelphia: Lippincott Williams and Wilkins.

ByHealthwise Staff
Primary Medical ReviewerE. Gregory Thompson, MD - Internal Medicine
Specialist Medical ReviewerMartin Steinberg, MD - Hematology
Last RevisedOctober 7, 2010

WebMD Medical Reference from Healthwise

Last Updated: October 07, 2010
This information is not intended to replace the advice of a doctor. Healthwise disclaims any liability for the decisions you make based on this information.

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