Article
Clinico-haematological profile of HbE syndrome in adults and children.
Hematology (Amsterdam, Netherlands) - 1 Feb 2004
Tyagi S, Pati H P, Choudhry V P, Saxena R
Abstract excerpt
Haemoglobin E beta thalassemia (HbE beta thalassemia) has a remarkable variability in clinical expression ranging from a mild form of thalassemia intermedia to a transfusion dependent condition. An overlap between the mild variety of HbE beta thalassemia and homozygous HbE disease is common, howe...
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