J Lab Med Qual Assur.  2012 Dec;34(2):113-117.

A Case of Heterozygous alpha(+)-Thalassemia Diagnosed in a Korean Family by Using Multiplex Ligation-Dependent Probe Amplification

• Oh AC
• Lee JK
• Hong YJ
• Hong SI
• Yang SH
• Park CH
• Kim HJ
• Jo HS
• Chang YH

Abstract

Alpha-thalassemia (alpha-thalassemia), which is prevalent in the Mediterranean region, is caused by deficient synthesis of the alpha-globin chains. It is commonly caused by HBA1 and/or HBA2 gene deletion and is diagnosed by DNA sequence analysis. The proband was a 38-year-old woman who was found to have microcytic and hypochromic anemia on a routine health checkup. Results of the Hb electrophoresis (EP) and direct sequencing of the HBA1 and HBA2 genes were found to be normal. As multiplex ligation-dependent probe amplification (MLPA) for the HBA1 and HBA2 genes revealed heterozygous deletion, she was diagnosed with heterozygous alpha+-thalassemia. Although routine laboratory tests revealed similar findings in the proband's father, brother and niece, MLPA revealed heterozygous deletions of the HBA1 or HBA2 gene in her brother and niece. In summary, we report a case of heterozygous alpha+-thalassemia in a Korean family that was detected by MLPA. We recommend that patients with suspected hemoglobinopathies should be followed-up further with MLPA, especially when Hb EP shows a normal pattern.

Keyword

Alpha-thalassemia; Multiplex ligation-dependent probe amplification (MLPA); Hemoglobinopathies

MeSH Terms

alpha-Globins
alpha-Thalassemia
Anemia, Hypochromic
Electrophoresis
Fathers
Female
Gene Deletion
Hemoglobin A, Glycosylated
Hemoglobinopathies
Humans
Mediterranean Region
Multiplex Polymerase Chain Reaction
Sequence Analysis, DNA
Siblings
Hemoglobin A, Glycosylated
alpha-Globins