Abstract
We describe a Chinese newborn who was assumed to have α0-thalassemia (α0-thal) by determining the amount of Hb Bart’s (γ4) in the cord blood, but was later shown to have only α+-thal. Hb J-Wenchang-Wuming [α11(A9)Lys→Gln (AAG>CAG) (α2 or α1)] was mistaken for Hb Bart’s as both hemoglobin (Hb) variants have the same mobility.