Benign familial polycythaemia
AUTOR(ES)
Geary, C. G.
RESUMO
An English family suffering from thalassaemia minor is described. Three generations are affected, and all the affected members had a considerably raised red cell count in the presence of slight or moderate anaemia, obviously abnormal peripheral films, and only slightly reduced M.C.H.C. values; and each had a moderately raised haemoglobin A2 level, though foetal haemoglobin levels were normal.
