Molecular Characterization of Hb H and AEBart’s
Diseases in Thai Children: Phramongkutklao Hospital
Experiences
Boonchai Boonyawat MD*,
Apichat Photia MD**, Chalinee Monsereenusorn MD**,
Piya Rujkijyanont MD**, Chanchai Traivaree MD**
Affiliation :
* Division of Genetics, Department of Pediatrics, Phramongkutklao Hospital and College of Medicine, Bangkok, Thailand
** Division of Hematology/Oncology, Department of Pediatrics, Phramongkutklao Hospital and College of Medicine,
Bangkok, Thailand
Background : Alpha-thalassemia is a common genetic disorder in Thailand and is caused by either deletion or non-deletional
mutation of one or both α-globin genes. Inactivation of three α-globin genes causes Hb H disease and interaction of Hb H
disease with heterozygous Hb E results in AEBart’s disease.
Objective : The present study aimed to characterize the genotype of α-globin gene in 81 pediatric patients with Hb H and
AEBart’s diseases in Phramongkutklao Hospital, a tertiary care center for thalassemic patients in central Thailand.
Material and Method: Eighty one unrelated pediatric patients including 60 patients with Hb H disease and 21 patients with
AEBart’s disease were enrolled in our study. Mutation analysis was performed by multiplex gap-PCR, multiplex-ARMS and
direct DNA sequencing of both HBA1 and HBA2 genes, respectively.
Results : A total of 81 pediatric patients with Hb H and AEBart’s diseases who mainly lived in central Thailand were included
in the present study. Eight different α-thalassemia mutations interacting to produce seven genotypes of α-globin gene in
both Hb H and AEBart’s diseases were identified. The number of patients in the non-deletional form was higher than in the
deletional form for both Hb H (51.6% VS 48.4%) and AEBart’s diseases (52.4% VS 47.6%). The SEA deletion (--SEA) was the
most common (98.8%) α-thalassemia 1 mutation. While 3.7-kb deletion (-α3.7) was the most common (90%) α-thalassemia
2 deletion, Hb CS was the most common (90%) non-deletional a-thalassemia 2. Uncommon non-deletional α-thalassemia
2 mutation identified in our study were Hb QS, Hb PS and initiation codon mutation, respectively.
Conclusion : All of the α-thalassemia mutation in our pediatric patients with Hb H and AEBart’s diseases have been
characterized by the combination of molecular techniques including multiplex gap-PCR, multiplex-ARMS and DNA sequenc-
ing of HBA1 and HBA2 genes.
Keywords : molecular analysis, α-globin gene, Hb H disease, AEBart’s disease, Thai children
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