Literature DB >> 19373588

Frequency of alpha-globin gene triplications and their interaction with beta-thalassemia mutations.

Piero C Giordano1, Margaretha Bakker-Verwij, Cornelis L Harteveld.   

Abstract

Our protocol for specialized diagnostics includes routine alpha-globin gene analysis for all blood samples referred to our diagnostic laboratory. alpha-Globin gene triplication is found to be present in more than 1% of samples tested. Since all cases with single alpha-gene triplications are associated with normal hematological parameters, we assume that preselection does not bias our observation and that alpha-globin gene triplications should be expected at the same frequency in the unselected Dutch multiethnic population as well. We have compared the average hematological parameters of beta-thalassemia (beta-thal) carriers with those of carriers with an associated alpha-gene triplication. In all cases, a single additional alpha gene had a very limited effect on the beta-thal minor phenotypes.

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Year:  2009        PMID: 19373588     DOI: 10.1080/03630260902827684

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


  8 in total

1.  [Rapid detection of alpha-globin gene αααanti-3.7 triplets with droplet digital PCR].

Authors:  Xiao-Qian Gong; Xue-Huang Yang; Lin-Li Qiao; Ya-Jun Cheng; Wan-Jun Zhou
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2017-09-20

2.  The Frequency of α-Globin Gene Triplication in a Southern Chinese Population.

Authors:  Man-Yu Wu; Jian-Ying Zhou; Jian Li; Dong-Zhi Li
Journal:  Indian J Hematol Blood Transfus       Date:  2015-09-02       Impact factor: 0.900

3.  Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the disease.

Authors:  Catherine Badens; Philippe Joly; Imane Agouti; Isabelle Thuret; Katia Gonnet; Synda Fattoum; Alain Francina; Marie-Claude Simeoni; Anderson Loundou; Serge Pissard
Journal:  Haematologica       Date:  2011-07-26       Impact factor: 9.941

4.  Alpha-globin gene triplication and its effect in beta-thalassemia carrier, sickle cell trait, and healthy individual.

Authors:  Mohammad Hamid; Bijan Keikhaei; Hamid Galehdari; Alihossein Saberi; Alireza Sedaghat; Gholamreza Shariati; Marziye Mohammadi-Anaei
Journal:  EJHaem       Date:  2021-07-19

Review 5.  Abnormal haemoglobins: detection & characterization.

Authors:  Henri Wajcman; Kamran Moradkhani
Journal:  Indian J Med Res       Date:  2011-10       Impact factor: 2.375

6.  Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia.

Authors:  Orna Steinberg-Shemer; Jacob C Ulirsch; Sharon Noy-Lotan; Tanya Krasnov; Dina Attias; Orly Dgany; Ruth Laor; Vijay G Sankaran; Hannah Tamary
Journal:  Cold Spring Harb Mol Case Stud       Date:  2017-11-21

7.  The Frequency and Importance of Common α-globin Gene Deletions Among β-Thalassemia Carriers in an Iranian Population.

Authors:  Azam Moosavi; Ali M Ardekani
Journal:  Avicenna J Med Biotechnol       Date:  2017 Oct-Dec

8.  Molecular Basis of α-Thalassemia in Iran

Authors:  Atefeh Valaei; Morteza Karimipoor; Alireza Kordafshari; Sirous Zeinali
Journal:  Iran Biomed J       Date:  2018-01-01
  8 in total

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