Successful transfer to sulfonylurea therapy in an infant with developmental delay, epilepsy and neonatal diabetes (DEND) syndrome and a novel ABCC8 gene mutation

MeSH terms

• ATP-Binding Cassette Transporters / genetics*
• Diabetes Mellitus / drug therapy*
• Diabetes Mellitus / genetics
• Epilepsy / drug therapy*
• Epilepsy / genetics
• Humans
• Hypoglycemic Agents
• Infant, Newborn
• Male
• Mutation
• Potassium Channels, Inwardly Rectifying / genetics*
• Receptors, Drug / genetics*
• Sulfonylurea Compounds / therapeutic use*
• Sulfonylurea Receptors