Divergent phenotypes in siblings with identical novel mutations in the HNF-1α gene leading to maturity onset diabetes of the young type 3. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Knebel, Birgit; Mack, Susanne; Haas, Jutta; Herman-Friede, Mona; Lange, Simone; Schubert, Oliver; Kotzka, Jorg; Muller-Wieland, Dirk
• Is Part Of: BMC medical genetics. Volume 17:Issue 1(2016)
• Page Start: 1
• Page End: 6
• Publication Date: 2016-12
• Subjects: Maturity-onset diabetes of the young -- HNF1A-MODY -- HNF-1α -- Metabolic syndrome -- Metabolic challenge -- Phenotype variety; Medical genetics -- Periodicals; 616.04205
• DOI: 10.1186/s12881-016-0297-z
• Languages: English
• ISSNs: 1471-2350

Abstract

Abstract Background Maturity onset diabetes of the young (MODY) is an autosomal dominant form of non–insulin-dependent diabetes mellitus caused by mutations in at least 13 different genes. The hepatocyte nuclear factor (HNF )-1α gene is affected in the most common form (HNF1A-MODY [MODY3 ]). Case presentation We describe the co-inheritance of a novel heterozygous missense mutation c.1761C > G (p.Pro588Ala) with a novel complex deletion insertion mutation (c.1765_1766delinsGCCCGfs86*) in theHNF-1α gene among affected members of one family. Both mutations were present in the affected patients and neither was present in unaffected family members. The family had not only inheritance of MODY but also increased susceptibility to type 2 diabetes. Therefore one family member had classical type 2 diabetes including metabolic syndrome aggravated by a genetic predisposition in the form of HNF1A-MODY. Conclusion The presence of common type 2 diabetes features should not detract from the possibility of MODY in patients with a striking autosomal-dominant family history.