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Haematological change in sickle cell–haemoglobin C disease and in sickle cell-beta thalassaemia: a cohort study from birth

✍ Scribed by M. C. G. Stevens; G. H. Maude; M. Beckford; Y. Grandison; K. Mason; B. E. Serjeant; B. Taylor; J. M. Topley; G. R. Serjeant

Book ID
114710603
Publisher
John Wiley and Sons
Year
1985
Tongue
English
Weight
588 KB
Volume
60
Category
Article
ISSN
0007-1048

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✍ Bienzle, U. ;Kappes, R. ;Reimer, A. ;Feldheim, M. ;Tischendorf, F. W. ;Kohne, E. 📂 Article 📅 1983 🏛 Springer-Verlag ⚖ 354 KB

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