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Recurrent infections in sickle cell disease: haematological and immune studies

✍ Scribed by K. De Ceulaer; A. Pagliuca; M. Forbes; G.H. Maude; B.E. Serjeant; G.R. Serjeant


Book ID
115825030
Publisher
Elsevier Science
Year
1985
Tongue
English
Weight
342 KB
Volume
148
Category
Article
ISSN
0009-8981

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Clinical and haematological features of 20 patients of several Liberian ethnic groups with sickle cell-beta +-thalassaemia are reported. Haemoglobin analysis showed increased Hb A2 values, high Hb A levels (median 25%), variable amounts of Hb F and a slight imbalance of non alpha/alpha globin chain