Severe beta(0) thalassemia/hemoglobin E disease caused by de novo 22-base pair duplication in the paternal allele of beta globin gene

Am J Hematol. 2007 Jul;82(7):663-5. doi: 10.1002/ajh.20816.

Abstract

beta Thalassemia is a major public health concern in Southeast Asia. A prevention program has been implemented in Thailand comprising mass carrier screening and genetic testing. In this study, a Thai girl with severe beta thalassemia/hemoglobin (Hb) E disease was born from the mother with Hb E trait and the genotypically normal father. DNA sequencing revealed novel 22-bp tandem duplication in the paternal allele of beta globin gene, producing a severely truncated product. A short recurring nucleotide at the insertion site suggested a predisposition to this mutation. Therefore, spontaneous beta globin mutations occasionally occur in normal population. Its clinical significance is noteworthy in countries with high prevalence of beta thalassemia.

Publication types

  • Case Reports

MeSH terms

  • Alleles*
  • Base Pairing
  • Base Sequence
  • Fathers
  • Female
  • Gene Duplication*
  • Globins / genetics*
  • Hemoglobin E / genetics*
  • Hemoglobin E / metabolism*
  • Humans
  • Infant
  • Male
  • Molecular Sequence Data
  • beta-Thalassemia / classification
  • beta-Thalassemia / genetics*
  • beta-Thalassemia / metabolism
  • beta-Thalassemia / pathology*

Substances

  • Globins
  • Hemoglobin E