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JBM-Journal de Biologie Medical. 2018; 7 (27): 220-221
in French | IMEMR | ID: emr-202463

ABSTRACT

O-Arab hemoglobin, a rare variant of Hb related to a mutation in the HbA beta chain, is asymptomatic hemoglobinopathy in the heterozygous state and is well tolerated in the homozygous state. However, double heterozygosity or heterozygous composite can be in a severe clinical form hence the importance of diagnosis, both in genetic counseling and early management of patients. We report three cases of O-Arab heterozygous haemoglobinopathy discovered incidentally in the HbA1c assay by HPLC on ADAMS [Arkray®]

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