Literature DB >> 2129613

Sickle cell hemoglobin, beta-thalassemia and G6PD deficiency in tribes of Maharashtra, India.

V R Rao1, A C Gorakshakar.   

Abstract

The prevalence of sickle cell hemoglobin (HbS), beta-thalassemia trait and G6PD deficiency are reported in some important Gond related endogamous tribes in Maharashtra, India. The HbS gene frequency varies from 0.0530 to 0.1805, the beta-thal gene from 0 to 0.0283 and Gd- gene from 0.0189 to 0.1120. The Pardhan tribe has been identified as a high risk group for sickle cell diseases. Statistically significant differences are observed between tribes.

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Year:  1990        PMID: 2129613

Source DB:  PubMed          Journal:  Gene Geogr        ISSN: 0394-249X


  3 in total

1.  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

2.  Micro mapping the frequencies of beta thalassemia and sickle cell anemia in India: A way forward to plan control strategies.

Authors:  Reena Das
Journal:  Indian J Hum Genet       Date:  2012-05

3.  Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India - Country scenario.

Authors:  Malay B Mukherjee; Roshan B Colah; Snehal Martin; Kanjaksha Ghosh
Journal:  Indian J Med Res       Date:  2015-05       Impact factor: 2.375

  3 in total

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