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Congenital hyperinsulinism—A case of mild hypoglycemia in an adult, detected by family testing
Symptoms of mild hypoglycemia are easily overlooked especially when there are no complaints from the patients, but it could be a warning sign of an underlying genetic disease. Genetic testing for the entire family is a key step in neonatal hypoglycemia workup.
Autores principales: | Baleanu, Felicia, Taujan, Georgiana, Rosu, Mihaela, Kosmopoulou, Olga, Papadopoulou, Blerta Ioanna, Boros, Emese, Iconaru, Laura |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731303/ https://www.ncbi.nlm.nih.gov/pubmed/36514475 http://dx.doi.org/10.1002/ccr3.6636 |
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