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Heterogeneity of G6PD deficiency prevalence in Mozambique: a school-based cross-sectional survey in three different regions

BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked hereditary enzymatic abnormality that affects more than 400 million people worldwide. Most deficient individuals do not manifest any symptoms; however, several precipitant agents—such as fava intake, infections, or severa...

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Publicado en:Malar J
Autores principales: Galatas, Beatriz, Mabote, Lurdes, Simone, Wilson, Matambisso, Gloria, Nhamussua, Lidia, Mañú-Pereira, María del Mar, Menéndez, Clara, Saute, Francisco, Macete, Eusebio, Bassat, Quique, Alonso, Pedro, Aide, Pedro
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2017
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5248496/
https://ncbi.nlm.nih.gov/pubmed/28103889
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12936-016-1674-y
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