Volume 20, Issue 3 pp. 230-231
Mutation in Brief
Free Access

Large Family With Maturity-Onset Diabetes of the Young and a Novel V121I Mutation in HNF4A

Carole T. Monney

Carole T. Monney

Division Autonome de Génétique Médicale, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland

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Valérie Kaltenrieder

Valérie Kaltenrieder

Division Autonome de Génétique Médicale, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland

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Pascal Cousin

Pascal Cousin

Division Autonome de Génétique Médicale, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland

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Christophe Bonny

Christophe Bonny

Division Autonome de Génétique Médicale, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland

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Daniel F. Schorderet

Corresponding Author

Daniel F. Schorderet

Division Autonome de Génétique Médicale, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland

Division Autonome de Génétique Médicale, CHUV, 1011 Lausanne; SwitzerlandSearch for more papers by this author
First published: 21 August 2002
Citations: 5

Communicated by Haig H. Kazazian, Jr.

Online Citation: Human Mutation, Mutation in Brief #521(2001) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/521.pdf

Abstract

Maturity-onset diabetes of the young (MODY) is a subtype of early-onset diabetes mellitus which is characterized by autosomal dominant inheritance. Several genes are known to induce MODY : HNF4A/MODY1, GCK/MODY2, TCF1/MODY3, IPF1/MODY4, TCF2/MODY5 and NEUROD1/MODY6. We studied a Swiss family with 13 diabetic patients over 3 generations. The average age at diagnosis was 35 ± 15 years (7 subjects before 30). In addition, 2 individuals had an abnormal oral glucose tolerance. The mutation present in this family was located in the DNA binding domain of HNF4A, a strongly conserved region across almost all species, and segregated in all the MODY patients. Identification of this missense mutation allowed for presymptomatic diagnosis in the younger generations and will improve medical follow-up of the predisposed individuals. © 2002 Wiley-Liss, Inc.

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