Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screening

BACKGROUND: Glucose-6-phosphate dehydrogenase deficiency (G6PDd) newborn screening is still a matter of debate due to its highly heterogeneous birth prevalence and clinical expression, as well as, the lack of enough knowledge on its natural history. Herein, we describe the early natural clinical cou...

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Detalles Bibliográficos
Autores principales: Vela-Amieva, Marcela, Alcántara-Ortigoza, Miguel Angel, González-del Angel, Ariadna, Belmont-Martínez, Leticia, López-Candiani, Carlos, Ibarra-González, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913327/
https://www.ncbi.nlm.nih.gov/pubmed/33637102
http://dx.doi.org/10.1186/s13023-021-01693-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913327/
https://www.ncbi.nlm.nih.gov/pubmed/33637102
http://dx.doi.org/10.1186/s13023-021-01693-9

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