Article
A rare Hb H disease due to the - -(SEA) and 16.6 kb α-thalassemia-2 deletions.
Hemoglobin - 1 Jan 2012
Sroymora Suravee, Jindadamrongwech Sumalee, Butthep Punnee, Chuncharunee Suporn
Abstract excerpt
A 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.
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