| Literature DB >> 22211024 |
Vijay S Bhat, Kalyan Kumar Dewan, Patnam Rajagopalan Krishnaswamy.
Abstract
We report a case of a diabetic, heterozygote with near normal hematology, marginally low level of hemoglobin A(2)(HbA(2)) having an increased level of hemoglobin F(HbF) that was pancellularly distributed among the red cells. BioRad DiaSTAT measurements gave a high glycated hemoglobin A1c(HbA1c) of 31.5% and the BioRad Variant analyzer recorded an HbA1c value which was very low, in discordance with the detected blood glucose levels. Flow cytometry and polymerization chain reaction (PCR) based studies were carried out which revealed the case to be that of the common hereditary persistence of fetal hemoglobin (HPFH)-3, an Asian Indian mutation. Fructosamine estimation and HbA1c by Boronate affinity chromatography were able to resolve the discordant value detected and was able to confirm the diabetes status. The case would have been a diagnostic dilemma, if reported without correlation.Entities:
Keywords: Alkaline electrophoresis; Flow cytometry; Fluorescein isothiocyanate (FITC); Gap polymerization chain reaction (Gap-PCR); Glycated hemoglobin A1c(HbA1c); Hereditary persistence of fetal hemoglobin (HPFH); High performance liquid chromatography (HPLC)
Year: 2010 PMID: 22211024 PMCID: PMC3068770 DOI: 10.1007/s12291-010-0076-0
Source DB: PubMed Journal: Indian J Clin Biochem ISSN: 0970-1915