Thalassemia in Viet Nam.

Khanh Q Bach, Ha T T Nguyen, Thanh H Nguyen, Minh B Nguyen, Tri A Nguyen

Journal: Hemoglobin 2022;46(1):62-65

PMID: 35950578

Abstract

The population of Viet Nam, is 96.2 million, of which 13.8% are carriers of thalassemia genes. Thalassemia/hemoglobinopathies carriers exist at different frequencies in all 54 ethnic groups of the country. Gene carrier rate and globin gene mutation rate varies ethnically and topographically. The ethnic groups in the Northern Highland region have high rates of α- and β-thalassemia (α- and β-thal), while those in the Southern Middle region have high rates of α-thalassemia (α-thal) and Hb E (or codon 26) (: c.79G>A). The lowest is found in La Hu (0.23%), while the highest is found in Raglai (88.6%). Thalassemia prevention and control programs were introduced using prenatal and neonatal diagnosis for the prevention of new thalassemic births. Most existing thalassemia patients are undergoing supportive treatment with regular blood transfusions and iron chelation. Curative treatment by hematopoietic stem cell transplantation is available but is limited to a minority of the patients.

Address: Thalassaemia Centre, National Institute of Hematology and Blood Transfusion, Hanoi, Viet Nam.

Link outs

Subscription / membership required

Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.