Clinico-haematological profiling of transfusion dependent and non transfucion dependent beta thalassaemia syndrome in Kedah

Introduction: β thalassaemia is a group of haemoglobin diseases caused by a reduction or absence in the synthesis of β globin chains. Affected individuals can be heterozygous, compound heterozygous, or homozygous for β thalassaemia, or even have interactions with other haemoglobinopathies. Kedah has...

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