ISSN:
1432-0584
Schlagwort(e):
Sickle cell-β+-thalassaemia
;
West Africa
;
Clinical and haematological features
Quelle:
Springer Online Journal Archives 1860-2000
Thema:
Medizin
Notizen:
Summary Clinical and haematological features of 20 patients of several Liberian ethnic groups with sickle cell-β+-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 a/a globin chain synthesis ratios. The clinical and other haematological findings varied but the disease seems to run a relatively mild course in the majority of the patients.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1007/BF00319897
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