| Literature DB >> 24826794 |
Andrew Turner1, Jurgen Sasse, Aniko Varadi.
Abstract
Hb Fontainebleau (HBA2: c.64G > C) is a rare α-globin variant, which has previously been described in only 10 individuals worldwide. We report here 12 additional cases identified in our laboratory. These included the first case of a homozygosity for Hb Fontainebleau and cases in which Hb Fontainebleau occurred in combination with deletional and nondeletional α-thalassemia (α-thal). The prevalence of Hb Fontainebleau in the samples submitted to our laboratory for premarital hemoglobinopathy screening was 0.24%, the highest reported prevalence to date, indicating that this is a comparatively common variant in the United Arab Emirates (UAE).Entities:
Keywords: Hb Fontainebleau; hemoglobinopathy; α-globin locus
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Substances:
Year: 2014 PMID: 24826794 DOI: 10.3109/03630269.2014.912221
Source DB: PubMed Journal: Hemoglobin ISSN: 0363-0269 Impact factor: 0.849