Manifestation of glucose-6-phosphate dehydrogenase deficiency in the wake of new-onset type 1 diabetes mellitus: a case report

BACKGROUND: Diabetes mellitus is the most common metabolic disease globally, while glucose-6-phosphate dehydrogenase deficiency, an X-linked inherited disorder, is the most common erythrocyte enzyme defect. The association between the two in children has been infrequently reported. CASE PRESENTATION...

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Detalles Bibliográficos
Autores principales: Govindarajan, Sandhya, Zamir, Imran, Bagewadi, Sunil, Moore, Emily
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414422/
https://www.ncbi.nlm.nih.gov/pubmed/36008815
http://dx.doi.org/10.1186/s13256-022-03549-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414422/
https://www.ncbi.nlm.nih.gov/pubmed/36008815
http://dx.doi.org/10.1186/s13256-022-03549-7

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