VIJAYAWADA: Sickle cell anaemia and thalassemia remain major ... stress that the only sustainable solution is to establish blood transfusion facilities in interior tribal areas.

Blood transfusions are a common medical procedure used to treat various conditions, including sickle ... of red blood cells, leading to severe anemia, often following a blood transfusion.

Given the remarkable advances seen with gene therapies for sickle cell disease (SCD ... One has been the move beyond simple transfusion to red blood cell exchanges (RBCX). If a patient receives ...

The clumps make red blood cells rigid and change their shape from flexible doughnuts into inflexible sickles – hence the name of the disease. Rigid sickle cells cannot travel through narrow ...

The resulting hemoglobin is called HbS. Rigid sickle cells cannot travel through narrow blood vessels, which clogs them, forming clots that stop blood circulation in different places. The clots ...

In children with sickle cell disease, regular blood transfusion (every 3-6 weeks) should be undertaken to maintain HbS at <25% and hemoglobin at 10-12.5 g/dl (B). After 3 years, a less-intensive ...

Gallbladder problems are a common complication in individuals with sickle cell disease. These issues often arise due to the breakdown of red blood cells and the subsequent formation of gallstones ...

Sickle cell anaemia is a genetic blood disorder characterised by the production of an abnormal haemoglobin, known as haemoglobin S. Sickle cell disease changes the shape of blood cells into a ...

Right now, approximately 20 billion red blood cells are busy travelling through your blood vessels. They are delivering oxygen to all the different tissues in your body and removing carbon dioxide to ...