Disseminated Histoplasmosis in a Brazilian Patient with G6PD Deficiency Caused by Class I Variant

Author:

Salgado Ranieri CoelhoORCID,Gomes Lillian Nunes,França Tábata Takahashi,da Silva Napoleão Sarah Maria,Barreiros Lucila Akune,de Oliveira Tiago Santos,Ishizuka Edson Kiyotaka,Ferreira Janaira Fernandes Severo,Condino-Neto Antonio

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Reference14 articles.

1. Siler U, et al. Severe glucose-6-phosphate dehydrogenase deficiency leads to susceptibility to infection and absent NETosis. J Allergy Clin Immunol. 2017;139:212–219.e3.

2. Richardson SR, O'Malley GF. Glucose-6-Phosphate Dehydrogenase Deficiency. 2022 Sep 26. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2023 Jan–. PMID: 29262208.

3. Jacobasch G, Bleiber R, Schönian G. Metabolism of the hexose monophosphate shunt in glucose-6-phosphate dehydrogenase deficiency and closely interrelated reactions. Haematologia (Budap). 1982;15:401–7.

4. Gong ZH, Tian GL, Huang QW, Wang YM, Xu HP. Reduced glutathione and glutathione disulfide in the blood of glucose-6-phosphate dehydrogenase-deficient newborns. BMC Pediatr. 2017;17:1–6.

5. Tarafdar A, Pula G. The role of NADPH oxidases and oxidative stress in neurodegenerative disorders. Int J Mol Sci. 2018;19:3824.

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