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Hb Zürich–Albisrieden, [α59(E8)Gly→Arg,  HBA1 : c.178G&gt;C] is a rare and highly unstable α-globin chain variant. The involved mutation has been reported in both  HBA1  and  HBA2  genes. A few compound heterozygotes of Hb Zürich–Albisrieden and α 0 -thalassemia have shown that this variant is associated with severe Hb H disease. We describe here another case of Hb Zürich–Albisrieden who presented with transfusion-dependent anemia beginning shortly after birth.

Severe Hb H Disease Caused by Hb Zürich–Albisrieden ( HBA1 : c.178G>C): Another Case Report