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β-Thalassemia mutations in subjects with borderline HbA2 values: a pilot study in North India
-
Aruna Rangan
,
Prashant Sharma
Published/Copyright:
September 6, 2011
Abstract
Background: Interpreting hemoglobin high performance liquid chromatograms with borderline HbA2 values is often problematic, especially in antenatal cases if the partner is a known thalassemia trait.
Methods: We tested for underlying β-thalassemia mutations in 25 subjects with borderline HbA2 values (between 3.0%–4.0%). Amplification refractory mutation system (ARMS-PCR) was used to detect the five common Indian β-thalassemia mutations: (IVS-I-5 (G>C), IVS-I-1 (G>T), codons 8/9 (+G), codons 41/42 (-TTCT) and 619 bp deletion). β-Globin gene sequencing was performed if no mutation was detected.
Results: A β-globin gene defect was identified in 8 (32%) of the 25 cases with HbA2 levels ranging from 3.5%–3.9%. ARMS-PCR revealed IVS-I-5 (G>C) in three, 619 bp deletion in two and codons 41/42 (-TTCT) in one case. Two cases had CAP +1 (A>C) mutation on gene sequencing. IVS-I-1 (G>T) and codons 8/9 (+G) were not found in this small cohort.
Conclusions: Mutation analysis should be offered to all at-risk couples with borderline HbA2, especially those with values between 3.5% and 4.0% and microcytic hypochromic indices. Significant mutations different from those in other ethnic populations were seen in this small institution-based study.
Received: 2011-2-10
Accepted: 2011-8-3
Published Online: 2011-9-6
Published in Print: 2011-12-1
©2011 by Walter de Gruyter Berlin Boston
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