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J Pediatr ; 150(5): 553-5, 2007 May.
Article in English | MEDLINE | ID: mdl-17452235

ABSTRACT

We describe a family in which 3/6 siblings had transient, relapsing neonatal diabetes. The father and another sibling had diabetes diagnosed at 20 and 9 years old, respectively. All affected individuals carried the same KCNJ11 gene mutation. In all, sulfonylurea treatment permitted cessation of insulin treatment, with improved glycemic control.


Subject(s)
Diabetes Mellitus/drug therapy , Glyburide/therapeutic use , Hypoglycemic Agents/therapeutic use , Adult , Child , Diabetes Mellitus/genetics , Female , Humans , Infant, Newborn , Male , Mutation , Pedigree , Potassium Channels, Inwardly Rectifying/genetics , Sulfonylurea Compounds/therapeutic use
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