Paper

Compound heterozygote of Hb DIran [HBB: c.67G>C, β 22(B4) Glu>Gln] with β0-thalassemia [cds 41/42 (-CTTT)] from Eastern India

Published Dec 1, 2017 · P. Mohanty, S. Meher, S. Dehury

Hematology, Transfusion and Cell Therapy

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Abstract

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Case Report

Study Snapshot

A rare combination of Hb DIran and 0-thalassemia mutations has been identified in Eastern India, resulting in a rare hemoglobin variant with a high risk of thrombosis.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Compound heterozygote of Hb DIran [HBB: c.67G>C, β 22(B4) Glu>Gln] with β0-thalassemia [cds 41/42 (-CTTT)] from Eastern India

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