Kobkorn PongjantharasatienWansa BanyatsuppasinSonnarong PounsawatSumalee JindadamrongwechMahidol University2018-12-112019-03-142018-12-112019-03-142016-07-03Hemoglobin. Vol.40, No.4 (2016), 283-2841532432X036302692-s2.0-84982933523https://repository.li.mahidol.ac.th/handle/123456789/42951© 2016 Informa UK Limited, trading as Taylor & Francis Group. α-Thalassemia (α-thal) is one of the most common genetic diseases in Thailand. Homozygosity of α-thal-1 (– –/– –) and compound heterozygosity of α-thal-1/α-thal-2 (– –/–α) leads to Hb Bart's (γ4) hydrops fetalis and Hb H (β4) disease, respectively. In order to better control and provide prevention of α-thal disease, the prevalence of α-thal-1 carriers and the types of genotypes in the Thai population should be known. A 7-year retrospective study, employing multiplex gap-polymerase chain reaction (gap-PCR) of 31,632 blood samples from Ramathibodi Hospital, Mahidol University, Bangkok, revealed an α-thal-1 carrier rate of 14.40% with the – –SEA(NG_000006.1: g.26264_45564del19301), – –THAI(NG_000006.1: g.10664_44164del33501) and – –FIL(NG_000006.1: g.11684_43534del31851) genotypes, constituting frequencies of 14.21, 0.18 and 0.01%, respectively. Although the – –FILgenotype is rare in the Thailand, its detection should be included in future α-thal screening programs.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyMedicineArticleSCOPUS10.1080/03630269.2016.1189932