Case Report: Hemoglobin H Disease with Compound Heterozygous -3.7 Deletion and Hb Constant Spring Mutation
Abstract Hemoglobin H (Hb H) disease is a moderate to severe form of alpha thalassemia resulting from impaired alpha globin production. We report a case of a patient with Hb H disease caused by compound heterozygosity for a deletional -3.7 mutation and a Hb Constant Spring (Hb CS) mutation. The patient presented with chronic anemia
