Clinica Chimica Acta 2012-10-09

Compromising for carrier detection of beta thalassemia based on measurement of HbA2 levels in unusual cases.

Stacy Colaco, Roshan Colah, K Ghosh, Anita Nadkarni

Index: Clin. Chim. Acta 413(19-20) , 1705-7, (2012)

Full Text: HTML

Abstract

An increased HbA2 level is the hallmark for identification of β thalassemia carriers. However, in some carriers the level of HbA2 is not typically elevated creating difficulties in making a diagnosis.We describe a family having an affected child referred to us for confirmation of diagnosis of β thalassemia.The father has a classical β thalassemia trait and the mother showed typical reduced red cell indices with a high RBC count but the HbA2 level was normal (2.4%). On molecular analysis she was a heterozygous carrier having IVS1 nt 5 (G→C) β thalassemia mutation. Further analysis of δ globin gene showed that the reduction in HbA2 was due to the presence of the δ mutation HbA2 Pelendri [CD 141(Leu→Pro, CTG→CCG)].The diagnosis of a β thalassemia carrier could have been compromised, and states the importance of comprehensive molecular analysis for accurate diagnosis in couples where one partner has β thalassemia trait.Copyright © 2012 Elsevier B.V. All rights reserved.