| Literature DB >> 22273484 |
Elisabeth Saller1, Kamran Moradkhani, Fabrizio Dutly, Isabelle Vinatier, Claude Préhu, Hannes Frischknecht, Michel Goossens.
Abstract
We report three cases with very heterogeneous Hb A(2) levels caused by known chromosomal rearrangements in the β-globin locus. These rearrangements had their breakpoints at the same region in the δ gene, leading either to the Senegalese δ(0)β(+)-thalassemia (δ(0)β(+)-thal) deletion or to an insertion of a δ gene, known as Anti-Lepore. One patient showed, apart from drastically increased Hb A(2) values of 17.0%, inconspicuous hematological values. He had an Anti-Lepore mutation with three copies of the δ gene, thus explaining the high Hb A(2) level. Two other patients had Hb A(2) levels in the lower borderline range and increased Hb F levels. Molecular analysis showed the Senegalese δ(0)β(+)-thal deletion. One of them presented with an additional mild β-thal mutation leading to β-thal intermedia. These cases illustrate that different gene rearrangements with the same breakpoints in the δ gene can lead to different levels of Hb A(2) depending on the remaining number of δ genes.Entities:
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Year: 2012 PMID: 22273484 DOI: 10.3109/03630269.2011.644651
Source DB: PubMed Journal: Hemoglobin ISSN: 0363-0269 Impact factor: 0.849