Diagnosis and Treatment of Neonatal Diabetes Caused by ATP-Channel Mutations: Genetic Insights, Sulfonylurea Therapy, and Future Directions

Background: Neonatal diabetes (NDM) is a rare genetic disorder diagnosed in infants under six months of age, characterized by persistent hyperglycemia resulting from insufficient or absent insulin production. Unlike the more common forms of diabetes, such as type 1 diabetes (T1D) and type 2 diabetes...

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Autori principali:	Michela Trada, Chiara Novara, Martina Moretto, Edoardo Burzi, Davide Tinti, Luisa De Sanctis
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	MDPI AG 2025-02-01
Serie:	Children
Soggetti:	neonatal diabetes KCNJ11 ABCC8 sulfonylureas genetic mutations ATP-sensitive potassium channels
Accesso online:	https://www.mdpi.com/2227-9067/12/2/219
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