{
  "abstract": "Maturity-onset diabetes of the young (MODY) is an autosomal dominant monogenic form of diabetes. This report describes a case with hepatocyte nuclear factor 1-alpha (HNF1A)-MODY due to a novel heterozygous HNF1A mutation. The patient presented with hyperglycaemia and glycosuria in the absence of diabetic ketoacidosis. Family history was notable for early-onset diabetes. Genetic testing confirmed a previously unreported pathogenic HNF1A variant. Treatment with a GLP-1 receptor agonist and metformin reduced glycated haemoglobin from 10.2% to 6.0% within 3 months. This case highlights the importance of genetic screening in early-onset diabetes, which is frequently misdiagnosed as type 1 or type 2 diabetes, and expands the spectrum of HNF1A mutations relevant to precision medicine.",
  "authors": [
    {
      "affiliations": [
        "Division of Endocrinology and Metabolism, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taipei, Taiwan"
      ],
      "name": "Yi-Chen Liu"
    },
    {
      "affiliations": [
        "Division of Endocrinology and Metabolism, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taipei, Taiwan"
      ],
      "name": "Sheng-Chiang Su"
    },
    {
      "affiliations": [
        "Division of Endocrinology and Metabolism, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taipei, Taiwan"
      ],
      "name": "Feng-Chih Kuo"
    },
    {
      "affiliations": [
        "Division of Endocrinology and Metabolism, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taipei, Taiwan"
      ],
      "name": "Yi-Jen Hung"
    },
    {
      "affiliations": [
        "Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taipei, Taiwan"
      ],
      "name": "Yen-Lin Chen"
    }
  ],
  "title": "Non-type 1 and non-type 2 diabetes in a young man due to novel mutation in HNF1A",
  "uid": "f2d1b8d6-4a40-5a3f-a589-bcaa762a14f9"
}