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Genotype-phenotype diversity of beta-thalassemia in Malaysia: treatment options and emerging therapies.

Authors
Type
Published Article
Journal
The Medical journal of Malaysia
Publication Date
Volume
65
Issue
4
Pages
256–260
Identifiers
PMID: 21901940
Source
Medline
License
Unknown

Abstract

The haemoglobinopathies and thalassemias represent the most common inherited monogenic disorders in the world. Beta-thalassaemia major is an ongoing public health problem in Malaysia. Prior to 2004, the country had no national policy for screening and registry for thalassemia. In the absence of a national audit, the true figure of the extent of thalassemia in the Malaysian population was largely presumptive from micro-mapping studies from various research workers in the country. The estimated carrier rate for beta-thalassemia in Malaysia is 3.5-4%. There were 4768 transfusion dependent thalassemia major patients as of May 2010 (Data from National Thalassemia Registry).

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