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2021, Vol: 8, Issue: 8
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    STATUS OF HB F IN SICKLE CELL ANAEMIC INDIVIDUALS OF YAVATMAL DISTRICT, MAHARASHTRA. (2020)
    Sandeep M. Chede, Dinesh D. Dabhadkar , Madhav M. Kalyankar , Alka M. Vikhar
    JCR. 2020: 3977 - 3980

    Abstract

    Sickle cell disease (SCD) is a major gene disorder among the tribal population of central India. Fetal Haemoglobin (HbF) is the best-known genetic modulator of sickle cell anaemia, which varies dramatically in concentration in the blood of these patients. The patients with SCA display a remarkable variability in the disease severity. Hence the objective of the present study was to determine the Fetal Haemoglobin (HbF) level in SCD patients (SS), carriers (AS) and normal individuals (AA). Studied population shows the highest HbF level in SS followed by AS individuals and a slightly higher HbF level in SS females than in their male counterparts. Among different age groups the highest HbF% was found in the age group of 11-20 years

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    Volume & Issue

    Volume 7 Issue-9

    Keywords

    Sickle cell disease (SCD), Fetal haemoglobin Hb F, Tribals, Yavatmal district.
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