[Drepanocytosis with alpha and beta(o) thalassemia: a case report]

C Désidéri-Vaillant1, J Olivro, E Valéro

  • 1Fédération des laboratoires, Hôpital d'instruction des armées Clermont Tonnerre, Brest.

We describe the case of a Sickle Cell Trait associated with alpha and beta(o) thalassemia at an young man without clinical abnormality. Capillary electrophoresis showed S haemoglobin at 67%, F haemoglobin at 29%, A2 haemoglobin at 4% and an absence of A haemoglobin. Accurate diagnosis was found by techniques of molecular biology.

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