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- W2284244427 abstract "BackgroundHyperinsulinemic hypoglycemia (HH) is the commonest cause of persistent hypoglycemia in the neonatal and infancy periods. HNF4A mutations are the third most common cause of diazoxide responsive congenital hyperinsulinism. Individuals carrying HNF4A mutations that result in familial monogenic diabetes later in life can present in early infancy with hyperinsulinism. The study was to describe a child associated with HH due to mutations in the HNF4A gene." @default.
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- W2284244427 date "2015-05-09" @default.
- W2284244427 modified "2023-09-22" @default.
- W2284244427 title "AB076. Congenital hyperinsulinism due to mutation of HNF4A: a case report." @default.
- W2284244427 doi "https://doi.org/10.3978/j.issn.2305-5839.2015.ab076" @default.
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