Sickle cell anaemia is a hereditary blood disorder.
It cannot be completely treated with medications. One can go for a bone marrow transplant which is a costly treatment. The rest is symptomatic treatment.
Sickle cell anaemia is characterised by abnormal red blood cells which are shaped like a sickle.
Such rbcs get destroyed easily. Anyone with ssa
can have 1.jaundice
2. Extreme and pain in the body
3.enlargement of spleen. Avoid iron