Prevalence of G6PD deficiency and knowledge of diagnosis in a sample of previously unscreened Lebanese males: clinical implications

Author:

Khneisser Issam1,Adib Salim M2,Loiselet Jacques1,Mégarbané André3

Affiliation:

1. Newborn Screening Laboratory, Medical Genetic Unit, Faculty of Medicine, Saint Joseph University, Beirut, Lebanon

2. Department of Epidemiology and Public Health, Faculty of Medicine, Saint-Joseph University, Beirut, Lebanon

3. Medical Genetic Unit, Faculty of Medicine, Saint Joseph University, Beirut, Lebanon

Abstract

The incidence of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Lebanon is estimated at 10 per 1000 in men and 0.4 per 1000 in women. A community-based cluster sampling survey was conducted in 15 villages in all areas in Lebanon. The survey found 36 cases of G6PD deficiency among 3000 men aged 14 years and above, yielding a cumulative incidence rate of 12 per 1000. Of those 36 cases, 28 (77.8%) knew of their problem since they had already suffered at least one severe anaemia crisis in their childhood following the ingestion of raw green fava beans. The remaining 22.2% were not aware at all of their defect. These findings confirm that G6PD is a common genetic problem in Lebanon. The efficiency of early screening programmes in terms of preventing severe, at times potentially lethal, haemolytic crises is currently being investigated.

Publisher

SAGE Publications

Subject

Public Health, Environmental and Occupational Health,Health Policy

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