Literature DB >> 20099666

[Congenital hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency].

M Mura1, R Saidi, A Wolf, J L Moalic, M Oliver.   

Abstract

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common enzyme defect with a wide range of clinical manifestations that can be severe. A variety of factors including many medications can induce hemolytic episodes. Screening for G6PD deficiency is required before use of some drugs especially primaquine or dapsone.

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Year:  2009        PMID: 20099666

Source DB:  PubMed          Journal:  Med Trop (Mars)        ISSN: 0025-682X


  1 in total

Review 1.  Prevalence, genetic variants and clinical implications of G-6-PD deficiency in Burkina Faso: a systematic review.

Authors:  Abdoul Karim Ouattara; Pouiré Yameogo; Lassina Traore; Birama Diarra; Maléki Assih; Tegwindé Rébéca Compaore; Dorcas Obiri-Yeboah; Serge Théophile Soubeiga; Florencia Wendkuuni Djigma; Jacques Simpore
Journal:  BMC Med Genet       Date:  2017-11-23       Impact factor: 2.103

  1 in total

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