Literature DB >> 23105893

Characterization of a hemoglobin variant: HbQ-India / IVS 1-1 [G>T]-β-thalassemia.

Vijay S Bhat1, K K Dewan, P R Krishnaswamy, A K Mandal, P Balaram.   

Abstract

Hemoglobin Q- India (alpha) 64 Asp → His is an alpha chain variant which is generally found in heterozygous state and presents normal hematological blood picture. Here we report a rare case of HbQ-India with a thalassemic phenotype that has been analyzed using a combination of mass spectrometry, gene sequencing and PCR analysis. This combined analyses revealed the HbQ variant to be associated with a beta chain mutation, IVS 1-1 [G>T]. Though HbQ has earlier been reported with thalassemic trait using different techniques, this is the first report of a compound α and β chain Hb heterozygous mutant involving HbQ and IVS1-1 being validated using Mass Spectrometry and Reverse dot blot hybridization.

Entities:  

Keywords:  Amplification Refractory Mutation System; Hemoglobin Q; Intervening sequence; Mass Spectrometry; Reverse dot blot hybridization

Year:  2010        PMID: 23105893      PMCID: PMC3453018          DOI: 10.1007/s12291-010-0020-3

Source DB:  PubMed          Journal:  Indian J Clin Biochem        ISSN: 0970-1915


  10 in total

1.  Rapid identification of hemoglobin variants by electrospray ionization mass spectrometry.

Authors:  B J Wild; B N Green; E K Cooper; M R Lalloz; S Erten; A D Stephens; D M Layton
Journal:  Blood Cells Mol Dis       Date:  2001 May-Jun       Impact factor: 3.039

Review 2.  Advanced analytical methods for hemoglobin variants.

Authors:  Yoshinao Wada
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2002-12-05       Impact factor: 3.205

3.  A haemoglobinopathy involving haemoglobin H and a new (Q) haemoglobin.

Authors:  F VELLA; R H WELLS; J A AGER; H LEHMANN
Journal:  Br Med J       Date:  1958-03-29

4.  Electrospray mass spectrometry in the clinical diagnosis of variant hemoglobins.

Authors:  C H Shackleton; A M Falick; B N Green; H E Witkowska
Journal:  J Chromatogr       Date:  1991-01-02

5.  HbQ-India in a Sindhi family: an uncommon hemoglobin variant.

Authors:  Devenkumar V Desai; Hiren Dhanani; Amit K Kapoor; Sashidhar V Yeluri
Journal:  Lab Hematol       Date:  2004

6.  Rapid analysis of hemoglobin variants by cation-exchange HPLC.

Authors:  C N Ou; C L Rognerud
Journal:  Clin Chem       Date:  1993-05       Impact factor: 8.327

7.  Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS).

Authors:  C R Newton; A Graham; L E Heptinstall; S J Powell; C Summers; N Kalsheker; J C Smith; A F Markham
Journal:  Nucleic Acids Res       Date:  1989-04-11       Impact factor: 16.971

8.  Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families.

Authors:  P K Sukumaran; S M Merchant; M P Desai; B G Wiltshire; H Lehmann
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318

9.  Two haemoglobins Q, alpha-74 (EF3) and alpha-75 (EF4) aspartic acid to histidine.

Authors:  P A Lorkin; D Charlesworth; H Lehmann; S Rahbar; S Tuchinda; L I Eng
Journal:  Br J Haematol       Date:  1970-07       Impact factor: 6.998

10.  Electrospray mass spectrometric characterization of hemoglobin Q (Hb Q-India) and a double mutant hemoglobin S/D in clinical samples.

Authors:  Amit Kumar Mandal; Shveta Bisht; Vijay S Bhat; Patnam Rajagopalan Krishnaswamy; Padmanabhan Balaram
Journal:  Clin Biochem       Date:  2007-09-21       Impact factor: 3.281

  10 in total
  1 in total

1.  Clinico-Hematological Profile of Hb Q India: An Uncommon Hemoglobin Variant.

Authors:  Aradhana Harrison; Ranjeet Singh Mashon; Naveen Kakkar; Sheila Das
Journal:  Indian J Hematol Blood Transfus       Date:  2017-08-18       Impact factor: 0.900

  1 in total

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