A rare Hb H disease due to the - SEA and 16.6 kb α-thalassemia-2 deletions

Suravee SroymoraSumalee JindadamrongwechPunnee ButthepSuporn ChuncharuneeFaculty of Medicine, Ramathibodi Hospital, Mahidol UniversityMahidol University2018-06-112018-06-112012-04-01Hemoglobin. Vol.36, No.2 (2012), 200-2041532432X036302692-s2.0-84858144713https://repository.li.mahidol.ac.th/handle/20.500.14594/13764A large deletional α-thalassemia-2 (α-thal-2) allele was identified in a Thai woman with Hb H disease. The proband has α-thal-1 (SEA type) in conjunction with a 16.6 kb deletion affecting the α2-globin allele. The proband had severe anemia and required a blood transfusion during puerperium. © 2012 Informa Healthcare USA, Inc.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyMedicineA rare Hb H disease due to the - SEA and 16.6 kb α-thalassemia-2 deletionsArticleSCOPUS10.3109/03630269.2012.655355