| 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. (05 Mar 2000) |
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| microdrepanocytic |
containing microcytic and drepanocytic elements, as in sickle cellthalassemia disease.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| microdrepanocytic d. |
sickle cellthalassemia d.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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