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- Title
A REVIEW ON SICKLE CELL ANEMIA.
- Authors
Vasaikar, Nita B.; Sonawane, Snehal; Patil, Swati; Borse, L. B.; Borse, S. L.; Pawar, S. P.
- Abstract
Sickle cell disease is a hereditary blood disorder. Characterized by abnormality in the oxygen carrying heamoglobin. It is characterized by various sign and symptoms sickle cell crisis, vasoocclusive the splenic sequestration crisis. The pathophysiology is related to the actual anemia of the illness is caused by heamolysis.for the diagnosis purpose in Hbss, the complete blood account reveals heamoglobin level in the range of 0.8g/dl. Managment are carried out by folic acid and penicillin, hydroxyl urea, transfusion therapy. Further research is needed on the relationship between this condition of sickle cell anemia.
- Subjects
SICKLE cell anemia; DISABILITY identification; PATHOLOGICAL physiology; BLOOD transfusion; VITAMIN B complex
- Publication
Pharma Science Monitor, 2015, Vol 6, Issue 2, p118
- ISSN
0976-9242
- Publication type
Article