Screening for Beta Thalassaemia Carriers: A Relook
نویسنده
چکیده
Thalasssaemia is an inherited disorder of haemoglobin synthesis. It is characterised by absence or reduced synthesis of one or more globin chains of human haemoglobin. Public health concern about carrier detection is not only confined to the geographical areas with high disease prevalence but becomes a global issue because of population migration [1]. The majority of carriers are not aware of their status. The homozygous state of β0-thalassaemia results in transfusion dependent thalassaemia.
منابع مشابه
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تاریخ انتشار 2015