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Abstract
We report a new hemoglobin (Hb) variant [β86(F2)Ala→Val; HBB:c.260C>T] that we have named Hb Izmir. We have identified Hb Izmir in a Turkish woman by ion exchange high performance liquid chromatography (HPLC) during a premarital screening program in the Aegean region of Turkey. The mother and sister of the proband also carried the same variant. Using direct sequencing, we have characterized this variant as resulting from a GCC>GTC replacement at codon 86 of the β-globin chain, corresponding to an Ala→Val amino acid substitution. In the heterozygote, the level of Hb Izmir ranged from 41.38 to 45.6%. All heterozygotes had a Hb A2 level of less than 3.5%. Total blood count values were normal and there were no other clinical findings. Although its clinical significance is thus far unclear, Hb Izmir may be important in hemoglobinopathy screening programs.
ACKNOWLEDGMENTS
The authors are grateful to the staff of the Ismail Cosar (BiocanTıp Laboratory, Istanbul, Turkey) and medical supplies (Primus Ultra2 system; Trinity Biotech, Kansas City, MO, USA) and the employees of The Ministry of Health of Turkey Local Health Authority of Mugla for their valuable contributions.
Declaration of Interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.