• Title of article

    Preimplantation Genetic Diagnosis for Beta Thalassemia

  • Author/Authors

    Khordadpoor Deilamani. Faravareh Tehran Medical Genetics laboratory, Tehran, Iran , Akbari, Mohammad Taghi Tehran Medical Genetics laboratory, Tehran, Iran

  • Pages
    5
  • From page
    1
  • To page
    5
  • Abstract
    Background: Beta thalassemia is an autosomal recessive genetic disease with the symptoms of severe anaemia, ineffective erythropoiesis and bone deformities. Preimplantation genetic diagnosis is a noninvasive clinical tool for couples who are at risk of affected pregnancy to have a healthy child. Objectives: Herewereport aPGDtest for a couplewhowere heterozygous for CD36/37(-T) mutation inHBBgene and had terminated one affected pregnancy. Methods: Haplotype analysis of 6 flanking STR markers as well as variant detection by cycle sequencing were included in our PGD test in order to investigate the status of the embryos reliably. Results: Three out of five embryos were transferable. Conclusions: One normal and one carrier embryo were transferred which resulted in the singleton pregnancy and the birth of a healthy girl.
  • Keywords
    Preimplantation Genetic Diagnosis , Beta Thalassemia , HBB
  • Journal title
    Journal of Human Genetics and Genomics
  • Serial Year
    2019
  • Record number

    2727771