Abstract
β-Thalassemia (β-thal) is a hereditary blood disorder characterized by the reduced or absent synthesis of β-globin chains. Here, we report a case of severe thalassemia with compound heterozygosity for a novel deletion mutation at codon 104 (–A) (HBB: c.313delA) and codons 41/42 (–CTTT) (HBB: c.126_129delCTTT) on the β-globin gene (HBB), and a coinheritance of the –α4.2 (leftward) deletion on the α-globin gene cluster. The proband was a 12-year-old boy, and four other family members were involved in this study. This novel frameshift mutation caused classical β-thal trait in the heterozygote and a transfusion-dependent form of β-thal major (β-TM) in compound heterozygosity with other β0 mutations.
Disclosure statement
The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.