A successful transition to sulfonylurea treatment in male infant with neonatal diabetes caused by the novel abcc8 gene mutation and three years follow-up. [electronic resource]
Producer: 20171214Description: 59-61 p. digitalISSN:- 1872-8227
- Child, Preschool
- Diabetes Mellitus, Type 1 -- diagnosis
- Diabetic Ketoacidosis -- diagnosis
- Drug Substitution
- Follow-Up Studies
- Humans
- Hypoglycemic Agents -- administration & dosage
- Infant
- Infant, Newborn
- Infant, Newborn, Diseases -- diagnosis
- Insulin -- administration & dosage
- Male
- Mutation
- Mutation, Missense
- Potassium Channels, Inwardly Rectifying -- genetics
- Sulfonylurea Compounds -- administration & dosage
- Sulfonylurea Receptors -- genetics
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Publication Type: Case Reports; Journal Article
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