Literature DB >> 8773089

Genetic epidemiology of the three predominant abnormal hemoglobins in India.

R S Balgir1.   

Abstract

Hemoglobinopathies in India are Important public health problems. Of the several abnormal of hemoglobin molecules, there are three variants, viz. Sickle cell, hemoglobin E and hemoglobin D which are predominantly prevalent in India. The cumulative gene frequencies of these hemoglobins have been found to be 5.35% in India. The average gene frequency of sickle cell and hemoglobin D in India has been observed to be 4.3% and 0.86%, respectively. In the North Eastern region of India, the gene frequency of hemoglobin E is 10.9%. Gene frequencies and spatial distribution of the predominant abnormal hemoglobins in India have been discussed in variance with the previous generalisations.

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Year:  1996        PMID: 8773089

Source DB:  PubMed          Journal:  J Assoc Physicians India        ISSN: 0004-5772


  19 in total

1.  Diversity of sickle cell trait in Jharkhand state in India: Is it the zone of contact between two geographically and ethnically distinct populations in India?

Authors:  Rachana Nagar; Rajiva Raman
Journal:  J Biosci       Date:  2015-09       Impact factor: 1.826

2.  Prenatal diagnosis of sickle cell disease by the technique of PCR.

Authors:  Praneeta J Singh; A C Shrivastava; A V Shrikhande
Journal:  Indian J Hematol Blood Transfus       Date:  2014-07-08       Impact factor: 0.900

3.  Spectrum of Haemoglobinopathies in a Tertiary Care Hospital of Armed Forces.

Authors:  G S Chopra; V Nair; P K Gupta; D K Mishra; A Sharma; O P Mathew
Journal:  Med J Armed Forces India       Date:  2011-07-21

4.  Efficacy of Dichlorophenolindophenol (DCIP) as Screening Test for Hb E: Revisited.

Authors:  Prakas Kumar Mandal; K S Nataraj; Shuvra Neel Baul; Malay Kumar Ghosh; Tuphan Kanti Dolai
Journal:  Indian J Hematol Blood Transfus       Date:  2019-12-04       Impact factor: 0.900

5.  Screening for the sickle cell gene in Chhattisgarh state, India: an approach to a major public health problem.

Authors:  Pradeep K Patra; Virander S Chauhan; Prafulla K Khodiar; Abdul R Dalla; Graham R Serjeant
Journal:  J Community Genet       Date:  2011-06-15

6.  Haemoglobinopathies and β-Thalassaemia among the Tribals Working in the Tea Gardens of Assam, India.

Authors:  Anju Barhai Teli; Rumi Deori; Sidhartha Protim Saikia
Journal:  J Clin Diagn Res       Date:  2016-12-01

7.  β-Thalassaemia and its Co-existence with Haemoglobin E and Haemoglobin S in Upper Assam Region of North Eastern India: A Hospital Based Study.

Authors:  Anju Barhai Teli; Rumi Deori; Sidhartha Protim Saikia; Kalyani Pathak; Rita Panyang; Rashmi Rajkakati
Journal:  J Clin Diagn Res       Date:  2016-04-01

8.  Phenotypic Diversity and Clinico-Hematological Profile of Hb E-Beta Thalassemic Children.

Authors:  Aditi Baruah; Mrinal Kumar Baruah
Journal:  Indian J Hematol Blood Transfus       Date:  2019-07-04       Impact factor: 0.900

9.  Double heterozygous for hemoglobin S and hemoglobin E - a case report from central India.

Authors:  A A Dani; A V Shrikhande
Journal:  Indian J Hematol Blood Transfus       Date:  2008-03-19       Impact factor: 0.900

10.  Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study.

Authors:  D Mohanty; R B Colah; A C Gorakshakar; R Z Patel; D C Master; J Mahanta; S K Sharma; U Chaudhari; M Ghosh; S Das; R P Britt; S Singh; C Ross; L Jagannathan; R Kaul; D K Shukla; V Muthuswamy
Journal:  J Community Genet       Date:  2012-10-21
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