Literature DB >> 24826794

Hb Fontainebleau (HBA2: c.64G > C) in the United Arab Emirates.

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

Mesh:

Substances:

Year:  2014        PMID: 24826794     DOI: 10.3109/03630269.2014.912221

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  3 in total

1.  First Report of Association Between Rare α-Thalassemia Mutation (HBA1: c.298A>T) and Hb Fontainebleau (HBA2: c.64G>C).

Authors:  Elham Ghadami; Ahmad Tamaddoni; Sadegh Sedaghat; Reza Tabaripour; Hadis Pourreza Baboli; Haleh Akhavan-Niaki
Journal:  Indian J Clin Biochem       Date:  2018-06-18

2.  Development and validation of a high throughput, closed tube method for the determination of haemoglobin alpha gene (HBA1 and HBA2) numbers by gene ratio assay copy enumeration-PCR (GRACE-PCR).

Authors:  Andrew Turner; Jurgen Sasse; Aniko Varadi
Journal:  BMC Med Genet       Date:  2015-12-18       Impact factor: 2.103

3.  First Observation of Hemoglobin G-Waimanalo and Hemoglobin Fontainebleau Cases in the Turkish Population.

Authors:  Duran Canatan; Türker Bilgen; Vildan Çiftçi; Gülsüm Yazıcı; Serpil Delibaş; İbrahim Keser
Journal:  Turk J Haematol       Date:  2016-03-05       Impact factor: 1.831

  3 in total

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