Literature DB >> 25576799

Diagnosis of a novel hemoglobinopathy of compound heterozygosity of hemoglobin S/hemoglobin Q India.

Sushama Parab1, Suhas Sakhare2, Caesar Sengupta1, Arokiaswamy Velumani1.   

Abstract

BACKGROUND: A novel double heterozygosity for the α chain variant Hb Q India and β chain variant Hb S is described. Hb S is prevalent in the central part of India while Hb Q India in its heterozygous state is found mainly in Sindhi families.
METHODS: Identification of both the variants, Hb S and Hb Q India, was done based on chromatograms of HPLC and capillary zone electrophoresis (CE). Confirmation of variants was done by PCR based amplification refractory mutation system (ARMS) technique.
RESULTS: Both HPLC and CE confirmed the presence of Hb S. HPLC showed a pointed narrow peak of Hb Q India at retention time of 4.55min while it is eluted in Hb D zone on CE. A hybrid variant of these α and β globin chains was eluted in Hb C window and Hb C zone on HPLC and CE respectively. Molecular studies using ARMS technique confirmed these findings. Both the cases showed positive sickling test and presented with mild anemia.
CONCLUSION: This is a unique 2 index cases for compound heterozygosity of Hb S with Hb Q India.
Copyright © 2015 Elsevier B.V. All rights reserved.

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Keywords:  Capillary electrophoresis; HPLC; Hb Q India; Hb S; Hemoglobinopathies

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Year:  2015        PMID: 25576799     DOI: 10.1016/j.cca.2014.12.037

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  1 in total

1.  A Novel Association of HbQ India Trait with Sickle Cell Anemia: a New Insight in Hemoglobinopathies.

Authors:  Rakesh K Gupta; Kartavya Kumar Verma; Gurmeet Singh
Journal:  SN Compr Clin Med       Date:  2022-01-04
  1 in total

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