Unexpected discovery of hemoglobinopathy C/β° thalassemia.

Wafaa Bouyarmane,Jean Uwingabiye,Asmaa Biaz,Achraf Rachid,Youness Mechal,Abdellah Dami,Sanae Bouhsain,Zhor Ouzzif,Samira El Machtani Idrissi

Clinical case reports（2018）

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摘要

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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