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References
Ahmed SG, Ibrahim VA (2002). Clinical significance of glucose-6-phosphate dehydrogenase deficiency in Nigerian patients with sickle cell disease. Nigerian Postgraduate Medical Journal 9(4):181-185. |
|
Benkerrou M, Alberti C, Couque N, Haouari Z (2013). Impact of glucoseâ€6â€phosphate dehydrogenase deficiency on sickle cell anaemia expression in infancy and early childhood: A prospective study. British Journal of Haematology 163(5):646-654. |
|
Bouanga JC, Mouélé R, Préhu C, Wajcman H, Feingold J (1998). Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Congo. Human Heredity 48(4):192-197. |
|
Cappellini MD, Fiorelli GE (2008). Glucose-6-phosphate dehydrogenase deficiency. The lancet 371(9606):64-74. |
|
Cotton F (2003). Contribution au diagnostic biochimique des maladies héréditaires de l'hémoglobine. Thèse Doctorat Université Libre de Bruxelles. Available at : |
|
Dahmani F, Saoud B, Jafaar K, Woumki A (2016). Etude de l'hémogramme dans la drépanocytose homozygote: à propos de 87 patients. The Pan African Medical Journal 25:240. |
|
Diagne I, Ndiaye O, Moreira C, Signate-Sy H, Camara B, Diouf S, Diack-Mbaye A, Ba M, Sarr M, Sow D, Fall M (2000). Les syndromes drépanocytaires majeurs en pédiatrie à Dakar (Sénégal). Archives de Pédiatrie 7(1):16-24. |
|
Diop S, Thiam D, Sene A, Cisse M, Fall K, Toure Fall AO, Sow O, Diakhate L (2000). Association drépanocytose-déficit en G-6-PD:-prévalence et influence sur le profil évolutif. Médecine d'Afrique Noire 47(7):321-326. |
|
Dolo A, Maiga B, Guindo A, Diakité SA, Diakite M, Tapily A, Traoré M, Sangaré B, Arama C, Daou M, Doumbo O (2014). Fréquence du déficit en glucose-6-phosphate déshydrogénase (A-376/202) dans trois groupes ethniques vivant en zone d'endémie palustre au Mali Frequency of Glucose-6-phosphate dehydrogenase deficiency (A-376/202) in three Malian ethnic groups. Bulletin de la Société de Pathologie Exotique 107(3):165-170. |
|
Gentilini M (1993). Enzymopathie érythrocytaire. Médecine Tropicale, Flammarion Eds, Paris, France. pp. 532-537. |
|
Jolly D (2000). Le déficit en G6PD: une affection génétique fréquente et mal connue: un cas d'école en santé publique. Flammarion médecine-sciences. Available at: |
|
Joseph R, Ho LY, Gomez JM, Rajdurai VS, Sivasankaran S, Yip YY (1999). Mass newborn screening for glucose-6-phosphate dehydrogenase deficiency in Singapore. The Southeast Asian Journal of Tropical Medicine and Public Health 30(2):70-71. |
|
Nacoulma E, Sakande J, Kafando E, Kpowbié ED, Guissou IP (2006). Profil hématologique et biochimique des drépanocytaires SS et SC en phase stationnaire au Centre Hospitalier National Yalgado Ouedraogo de Ouagadougou. Mali Medical 21(1):8-11. |
|
Nouraie M, Reading NS, Campbell A, Minniti CP, Rana SR, Luchtmanâ€Jones L, Kato GJ, Gladwin MT, Castro OL, Prchal JT, Gordeuk VR (2010). Association of G6PD202A, 376G with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia. British Journal of Haematology 150(2):218-225. |
|
Shongo M, Mukuku O, Mutombo A, Loubala T (2015). Hematological and nutritional profile of SS homozygous sickle cell aged 6-59 months in Lubumbashi, Democratic Republic of Congo. Pan African Medical Journal 21(1):276. |
|
Vizzi A, Bastisdas G, Hidalgo M, Colman L, Perez HA (2016). Prevalence and molecular characterization of G6PD deficiency in two Plasmodium vivax endemic areas in Venezuela: predominance of the African A-202A/376G variant. Malaria Journal 15(1):19. |
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