A Formula to Identify Potential Cases of β-Thalassemia/HbE Disease Among Patients With Absent HbA, HbE >75% and HbF Between 5 and 15%

Author:

Pornprasert Sakorn1,Tookjai Monthathip2,Punyamung Manoo2,Kongthai Kanyakan3

Affiliation:

1. Department of Medical Technology, Faculty of Associated Medical Sciences and Chiang Mai University, Thailand

2. Associated Medical Sciences Clinical Service Center, Faculty of Associated Medical Sciences and Chiang Mai University, Thailand

3. Chiang Mai Health Promoting Hospital, Thailand

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

Reference22 articles.

1. Clinical manifestation of beta-thalassemia/hemoglobin E disease;Fucharoen;J Pediatr Hematol Oncol,2000

2. Variable severity of Southeast Asian beta 0-thalassemia/Hb E disease;Fucharoen;Birth Defects Orig Artic Ser,1987

3. Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-β-thalassemia in Northeast Thailand;Nuntakarn;Blood Cells Mol Dis,2009

4. Haemoglobinopathies in southeast Asia;Fucharoen;Indian J Med Res,2011

5. Screening for thalassemia and hemoglobinopathy in a rural area of Thailand: a preliminary study;Nathalang;J Med Assoc Thai,2005

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