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Unexpected discovery of hemoglobinopathy C/β° thalassemia

Clinical Case Reports (2018) 6(11) 2117-2120
DOI: 10.1002/ccr3.1815
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Abstract

High performance liquid chromatography (HPLC) is the current method of choice for the detection of hemoglobinopathies and the quantification of A2 and fetal hemoglobin. We are describing a case where a double heterozygosity C/beta-thalassemia was fortuitously identified, during assaying HBA1c, by HPLC.

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Bouyarmane, W., Uwingabiye, J., Biaz, A., Rachid, A., Mechal, Y., Dami, A., … El Machtani Idrissi, S. (2018). Unexpected discovery of hemoglobinopathy C/β° thalassemia. Clinical Case Reports, 6(11), 2117–2120. https://doi.org/10.1002/ccr3.1815

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