• ISSN: 2349-6002
  • UGC Approved Journal No 47859

Sickle cell anemia

  • Unique Paper ID: 152270
  • Volume: 8
  • Issue: 2
  • PageNo: 871-873
  • Abstract:
  • This paper reviews Sickle cell anemia. Sickle cell anemia is a homozygous form of HbS (HbSS).from one place instead of glutamine with valine in place 6 of the ye- globin chain.the cells also lead to polymerization and vaso-occlussion in the vasculature. Type β - globin is found inshort arm of chromosome 11. The combination of two tununts ant-globin subunits form hemoglobin S (HbS). Less -oxygen conditions, the absence of polar amino acids in the sixth ye-globin chain promotes diversityhemoglobin polymerization, which reverses red blood cells and then cuts and reduces their stiffness.

Cite This Article

  • ISSN: 2349-6002
  • Volume: 8
  • Issue: 2
  • PageNo: 871-873

Sickle cell anemia

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