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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2023
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| 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 |