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[Association of hemoglobinosis D-Punjab and β-thalassemia in a Moroccan family].
Ann Biol Clin (Paris)
February 2020
Service de biochimie-toxicologie, Hôpital militaire d'instruction Mohammed V, Rabat, Maroc, Faculté de médecine et de pharmacie, Université Mohammed V de Rabat, Maroc.
Unlabelled: Hemoglobin D-Punjab is a common hemoglobin variant in India but very rare in Morocco. Often, its presence has minimal or no clinical impact. Its heterozygous association with β-thalassemia is exceptional.
View Article and Find Full Text PDFThirty-two cases of HbS hemoglobinosis diagnosed in nine families of Romania are reported. Of these 26 were HbS trait carriers and 6 were double heterozygous presenting an association of HbS and beta-thalassemia. In the latter, one of the patients was carrier of HbS and the other had minor thalassemia with increased values of HbA2.
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