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Also known as: sickle cell anaemia Β· vaso-occlusive crisis Β· SCD
An inherited haemoglobinopathy (HbS) causing chronic haemolytic anaemia and painful vaso-occlusive crises, with risks of infection, acute chest syndrome, stroke and cumulative organ damage.
Inherited (autosomal recessive); common in African and in some central-Indian/tribal populations; crises triggered by infection, dehydration, cold, hypoxia and stress.
Vaso-occlusive crisis
Crisis prevention and disease-modification
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