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.

Detalles Bibliográficos
Autores principales: Baleanu, Felicia, Taujan, Georgiana, Rosu, Mihaela, Kosmopoulou, Olga, Papadopoulou, Blerta Ioanna, Boros, Emese, Iconaru, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
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

Internet

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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