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Mutations in the KCNJ11 gene are associated with MODY13, transient neonatal diabetes mellitus type 3 (TNDM3), permanent neonatal diabetes mellitus (PNDM), familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), and also contributes to an autosomal dominant form of type 2 diabetes

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doi: 10.1055/s-2000-9907

It should also be avoided in those with an increased risk of aspiration, uncontrolled vomiting, or coingestion of a corrosive or proconvulsant

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