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Spectrum of Haemoglobinopathies in a Suburb of Indore (India): A Two Year Study

Anjali Singh , Sanjeev Narang* , Anjali Singh** , Shrikant Nema***

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Indian Journal of Pathology: Research and Practice 6(2 (Part-2)):p 378-382, APRIL - JUNE 2017. | DOI: DOI: http://dx.doi.org/10.21088/ijprp.2278.148X.62(pt-II)17.6

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Abstract

Hemoglobinopathiesare monogenic disorders of erythrocyte production. We present an observational study of 200 anaemic patients at a tertiary health care center presented over two years (January 2015 to December 2016). Sickle-thalassemia was the most common form of haemoglobinopathy (56.4%), followed by β-thalassemia carrier (16.6%), Sickle cell trait (15.3%) β-thalassemia (10.2%), & Sickle cell disease (1.28%), respectively. Almost equal incidence in male and female were found. The maximum number of cases came to attention in the age group of 6-15 years followed by those in the age group of 16-30 years.

Keywords: Haemoglobinopathy; Sickle Thalassemia; β-Thalassemia; β-Thalassemia Carrier.

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DOI: DOI: http://dx.doi.org/10.21088/ijprp.2278.148X.62(pt-II)17.6

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