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KATP channel mutations in infants with permanent diabetes diagnosed after 6 months of life

10 Oct 2011

Abstract excerpt

BACKGROUND/OBJECTIVE: Mutations in the K(ATP) channel genes are the commonest cause of permanent neonatal diabetes. Most patients obtain optimal glycemic control on sulfonylurea treatment. Genetic testing is currently recommended for all infants diagnosed before 6 months of age. We aimed to explore the prevalence of K(ATP) channel diabetes in infants presenting between 6 and 12 months. METHODS: The KCNJ11 and...

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PMID: 21981029
DOI: 10.1111/j.1399-5448.2011.00824.x

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KATP channel mutations in infants with permanent diabetes diagnosed after 6 months of lifePMID 21981029Read ↗

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