Glutamate dehydrogenase hyperinsulinism: mechanisms, diagnosis, and treatment

Congenital hyperinsulinism (CHI) is a genetically heterogeneous disease, in which intractable, persistent hypoglycemia is induced by excessive insulin secretion and increased serum insulin concentration. To date,15 genes have been found to be associated with the pathogenesis of CHI. Glutamate dehydr...

Descripción completa

Detalles Bibliográficos
Autores principales: Zeng, Qiao, Sang, Yan-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887739/
https://www.ncbi.nlm.nih.gov/pubmed/36721237
http://dx.doi.org/10.1186/s13023-023-02624-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887739/
https://www.ncbi.nlm.nih.gov/pubmed/36721237
http://dx.doi.org/10.1186/s13023-023-02624-6

Ejemplares similares