Hemoglobin sickle-beta thalassemia
Other Names for this Disease
- Hb S beta-thalassemia
- Sickle beta thalassemia
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sickle cell anemia. This condition occurs when an individual inherits two altered HBB genes -- one from a parent who is a carrier of beta thalassemia and and the other from a parent who is a carrier of sickle cell anemia. This condition is inherited in an autosomal recessive fashion and is caused by mutations in the hemoglobin, beta (HBB) gene.Hemoglobin sickle-beta thalassemia, also known as sickle beta thalassemia and sickle cell-beta thalassemia, is considered a variant form of
Last updated: 4/14/2011
- Beta Thalassemia. Cooley's Anemia Foundation. http://www.cooleysanemia.org/updates/pdf/Beta_Thalassemia.pdf. Accessed 4/14/2011.
- Bender MA & Hobbs W. Sickle Cell Disease. GeneReviews. May 17, 2012; http://www.ncbi.nlm.nih.gov/books/NBK1377/. Accessed 12/20/2012.
- Genetics Home Reference (GHR) contains information on Hemoglobin sickle-beta thalassemia. This website is maintained by the National Library of Medicine.
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- The Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
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