Hb Q ? India: An uncommon hemoglobin variant diagnosed in two patients ? Case series
Journal: International Archives of Integrated Medicine (IAIM) (Vol.1, No. 4)Publication Date: 2014-12-19
Authors : Rippalkumar Bhimani; Gunvanti B. Rathod; Sachin Aggarwal; Rushabh Patel; Rahul Goyal; N.K. Kuchhal;
Page : 68-74
Keywords : Hemoglobin Q-India; Hemoglobinopathy; Aspartic acid; Histidine.;
Abstract
Hemoglobin Q-India (α 64 Asp→His) is an important member of the hemoglobin Q family, molecularly characterized by the replacement of aspartic acid by histidine. The first case of Hb Q-India was reported by Sukumaran in 1972 in a Sindhi family with associated β-Thalassemia. India is known as a country with a high prevalence of α - and β-thalassemia and different types of hemoglobinopathy. Many of these variants are yet to be identified. Here, we are reporting two cases of Hb Q- India diagnosed during premarital thalassemia screening.
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Last modified: 2014-12-22 15:30:18