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microdrepanocytic anaemia (medicine)


microdrepanocytic anaemia
Anaemia, clinically resembling sickle cell anaemia, in which individuals are compound heterozygous for the sickle cell gene and a thalassaemia gene; about 60 to 80% of haemoglobin is Hb S, up to 20% Hb F, and the remainder Hb anaemia.

Synonym: sickle cell-thalassaemia disease.