Prevention and control of thalassemia in Asia.

dc.contributor.authorFucharoen, Suthat
dc.contributor.authorWinichagoon, Pranee
dc.date.accessioned2011-11-04T07:42:33Z
dc.date.available2011-11-04T07:42:33Z
dc.date.issued2007-06
dc.description.abstractThalassemia and abnormal hemoglobin are the most common inherited diseases. The only treatment readily available in most countries is regular blood transfusion and iron chelation that is recommended in severely anemic patients with iron overload. In the last 20 years there has been much progress in terms of diagnosing, preventing and managing thalassemia. This has lead to the success of prevention and control of thalassemia in many Mediterranean countries such as Cyprus, Italy and Greece. Objective: To introduce approaches that may be applied for the control of thalassemia in developing countries including Asia where thalassemias are very prevalent.en_US
dc.identifier.citationAsian Biomedicine (Research Reviews and News); Vol. 1 No. 1 June 2007; 1-6.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/135135
dc.language.isoenen_US
dc.source.urihttps://abm.digitaljournals.org/index.php/abm/article/viewFile/91/10en_US
dc.subjectAsiaen_US
dc.subjectpreventionen_US
dc.subjectthalassemiaen_US
dc.titlePrevention and control of thalassemia in Asia.en_US
dc.typeArticleen_US
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