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HandWiki. Alpha Thalassemia Abnormal Morphogenesis. Encyclopedia. Available online: https://encyclopedia.pub/entry/27937 (accessed on 21 September 2026).
HandWiki. Alpha Thalassemia Abnormal Morphogenesis. Encyclopedia. Available at: https://encyclopedia.pub/entry/27937. Accessed September 21, 2026.
HandWiki. "Alpha Thalassemia Abnormal Morphogenesis" Encyclopedia, https://encyclopedia.pub/entry/27937 (accessed September 21, 2026).
HandWiki. (2022, September 29). Alpha Thalassemia Abnormal Morphogenesis. In Encyclopedia. https://encyclopedia.pub/entry/27937
HandWiki. "Alpha Thalassemia Abnormal Morphogenesis." Encyclopedia. Web. 29 September, 2022.
Alpha Thalassemia Abnormal Morphogenesis
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Alpha Thalassemia-Abnormal Morphogensis is a group of blood disorders that affect the way the body makes hemoglobin. Hemoglobin is a protein found in red blood cells that carries oxygen throughout the body. It's made up of alpha globin and beta globin. Normally each person has four genes for alpha globin, Alpha thalassemia happens when one or more of the genes that control the making of alpha globin is absent or defective. It can cause anemia ranging from mild to severe. Also causing Genital abnormalities and terminal transverse limb defectiveness which is why it is called abnormal morphogenesis. This is most commonly found in people of African, Middle Eastern, Chinese, Southeast Asian and occasionally, Mediterranean descent.

hemoglobin red blood cells globin

References

  1. "beta thalassemia description". http://ghr.nlm.nih.gov/condition/beta-thalassemia. Retrieved November 3, 2015. 
  2. "Alpha Thalassemia". http://ghr.nlm.nih.gov/condition/alpha-thalassemia. Retrieved 30 October 2015. 
  3. "Alpha thalassemia". http://ghr.nlm.nih.gov/condition/alpha-thalassemia. Retrieved November 3, 2015. 
  4. Miller, MD, Robin. "Alpha Thalassemia". http://kidshealth.org/parent/medical/heart/thalassemias.html#. Retrieved 30 October 2015. 
  5. Harteveld, Cornelis L.; Higgs, Douglas R.. "A-thalassaemia". 
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Subjects: Cell Biology
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Update Date: 29 Sep 2022
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