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Volume 2
July 24-25, 2019 | Rome, Italy
World Hematology 2019 & Nursing Care 2019
July 24-25, 2019
Journal of Blood Disorders and Treatment
47
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WORLD CONGRESS ON NURSING CARE
11
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WORLD HEMATOLOGY AND ONCOLOGY CONGRESS
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Prevalance of thalassemia syndromes, hemoglobinopathies and mutation analysis in a
tribal school in India
Amarinder Oberoi, Swati Kanakia
Lilavati Hospital and Research Centre, India
Introduction
: Thalassemia and other hemoglobinopathies are the most common monogenic disorders in India with a high
prevalence in tribal populations.
Aims and Objectives
: To detect the prevalence of thalassemia syndromes and sickle cell anemia in a tribal school population of
adolescent age group and mutation analysis of the positive cases.
Materials andMethods
: This study was conducted on 211 children aged 10-14 years from a tribal school in the state Maharashtra,
India. After taking clinical history, complete hemogram report was obtained by an automated cell counter. High-performance
liquid chromatography (HPLC) was performed on the samples with Bio Rad D-10™ Analyser. The samples with abnormal
electrophoresis patterns were subjected to next generation sequencing of HBH gene for mutation analysis.
Results
: Of the 211 students sampled, 193 (91.5%) had a normal electrophoresis pattern and abnormalities were detected in 18
(8.5%) cases. β (beta) thalassemia trait was the commonest abnormality found in 16 (7.6 %) children. Heterozygous sickle cell
and alpha thalassemia were found in 1 (0.5%) case each.
Of the 16 Thalassemia traits, 13 (81.25%) had IVS1-5(G>C) mutation, followed by c.47G>A (p. Trp16Ter) in 2 students (12.5%)
and IVS1-1(G>T) c.92+1G>T in 1student (6.25%). The one sickle heterozygote had c.20A>T (p. Glu7Val) mutation.
Conclusion
: High frequencies of these mutant alleles are maintained by the tribal populations probably due to consanguinity,
lack of awareness and conveyance; low income status and high cost of treatment make them vulnerable. These groups must
undergo premarital screening to decrease the risk bearing offspring with hemoglobinopathies.
Biography
Amarinder Oberoi is a pediatric resident with a keen interest in community pediatrics and genetics. After graduation he has worked in
a rural hospital with bare minimum facilities for a year. Currently in final year of residency plans to pursue further studies in neurology
or hematology.
karanwicked@gmail.comJ Blood Disord Treat, Volume 2