Abnormal Hemoglobins (HbD and HbQIndia) and β-Thalassaemia among the Indian Sindhis
- *Corresponding Author:
- Dipika Mohanty
Senior Consultant Haematologist and Chief of Laboratory Services
Apollo Hospitals, Plot No 251, Old Sainik School Road
Bhubaneswar, Odisha, India – 750015
E-mail: [email protected]
Received Date: April 28, 2013; Accepted Date: May 14, 2013; Published Date: May 24, 2013
Citation: Das K, Dhas P, Sahu PN, Rao VR, Mohanty D (2013) Abnormal Hemoglobins (HbD and HbQIndia) and ß-Thalassaemia among the Indian Sindhis. Hereditary Genetics S1:008. doi: 10.4172/2161-1041.S1-008
Copyright: © 2013 Das K, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
The Sindhi is one of the largest linguistic communities, migrated about 65 years back from the Sind province of West Pakistan to India. Though they share so many common practices with the Punjabis (especially those from Multan) and Gujarati Lohanas restricted endogamy and occupational specificity among this community is prominent . Linguistically the community has been classified under the Indo-European linguistic sub-division and racially proximity has been postulated with the Mediterranean and Alpo-Dinarics. Earlier investigation among the Sindhis of Nagpur city has revealed the existence of a number of subgroups with marked territorial identity and these subgroups were found to be heterogeneous with respect to selected sero-genetic loci .