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The conundrum in diagnosing Maturity-Onset Diabetes of the Young (MODY) in a large German pedigree with early-onset diabetes and a novel HNF1A variant.

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Title: The conundrum in diagnosing Maturity-Onset Diabetes of the Young (MODY) in a large German pedigree with early-onset diabetes and a novel HNF1A variant.
Authors: Giannopoulou EZ; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.; Center for Rare Endocrine Diseases at the University of Ulm, Ulm, Germany., Moawia A; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany., Högel J; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany., Lerner J; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.; Center for Rare Endocrine Diseases at the University of Ulm, Ulm, Germany.; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany., Zorn S; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.; Center for Rare Endocrine Diseases at the University of Ulm, Ulm, Germany.; German Center for Child and Adolescent Health (DZKJ), Partner Site Ulm, Ulm, Germany., Denzer C; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.; Center for Rare Endocrine Diseases at the University of Ulm, Ulm, Germany., Siebert R; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.; German Center for Child and Adolescent Health (DZKJ), Partner Site Ulm, Ulm, Germany., Wabitsch M; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany. Martin.Wabitsch@uniklinik-ulm.de.; Center for Rare Endocrine Diseases at the University of Ulm, Ulm, Germany. Martin.Wabitsch@uniklinik-ulm.de.; German Center for Child and Adolescent Health (DZKJ), Partner Site Ulm, Ulm, Germany. Martin.Wabitsch@uniklinik-ulm.de.
Source: Molecular and cellular pediatrics [Mol Cell Pediatr] 2026 Apr 10; Vol. 13 (1). Date of Electronic Publication: 2026 Apr 10.
Publication Type: Journal Article
Journal Info: Publisher: Springer Country of Publication: Germany NLM ID: 101660689 Publication Model: Electronic Cited Medium: Print ISSN: 2194-7791 (Print) Linking ISSN: 21947791 NLM ISO Abbreviation: Mol Cell Pediatr Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: The conundrum in diagnosing Maturity-Onset Diabetes of the Young (MODY) in a large German pedigree with early-onset diabetes and a novel HNF1A variant.
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  Data: <searchLink fieldCode="AU" term="%22Giannopoulou+EZ%22">Giannopoulou EZ</searchLink>; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.; Center for Rare Endocrine Diseases at the University of Ulm, Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Moawia+A%22">Moawia A</searchLink>; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Högel+J%22">Högel J</searchLink>; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Lerner+J%22">Lerner J</searchLink>; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.; Center for Rare Endocrine Diseases at the University of Ulm, Ulm, Germany.; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Zorn+S%22">Zorn S</searchLink>; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.; Center for Rare Endocrine Diseases at the University of Ulm, Ulm, Germany.; German Center for Child and Adolescent Health (DZKJ), Partner Site Ulm, Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Denzer+C%22">Denzer C</searchLink>; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.; Center for Rare Endocrine Diseases at the University of Ulm, Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Siebert+R%22">Siebert R</searchLink>; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.; German Center for Child and Adolescent Health (DZKJ), Partner Site Ulm, Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Wabitsch+M%22">Wabitsch M</searchLink>; Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany. Martin.Wabitsch@uniklinik-ulm.de.; Center for Rare Endocrine Diseases at the University of Ulm, Ulm, Germany. Martin.Wabitsch@uniklinik-ulm.de.; German Center for Child and Adolescent Health (DZKJ), Partner Site Ulm, Ulm, Germany. Martin.Wabitsch@uniklinik-ulm.de.
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              Text: 2026 Apr 10
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