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A Case of Maturity Onset Diabetes of the Young (MODY3) in a Family with a Novel HNF1A Gene Mutation in Five Generations
Diabetes mellitus with autosomal dominant inheritance, i.e., maturity-onset diabetes of the young (MODY), is a genetic form of diabetes mellitus. The MODY phenotype is associated with gene mutations leading to pancreatic β-cell dysfunction. Here, we present the clinical case of a 50-year-old proband...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Healthcare
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801236/ https://www.ncbi.nlm.nih.gov/pubmed/29222740 http://dx.doi.org/10.1007/s13300-017-0350-8 |
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author | Ovsyannikova, A. K. Rymar, O. D. Ivanoshchuk, D. E. Mikhailova, Svetlana V. Shakhtshneider, E. V. Orlov, P. S. Malakhina, E. S. Voevoda, M. I. |
author_facet | Ovsyannikova, A. K. Rymar, O. D. Ivanoshchuk, D. E. Mikhailova, Svetlana V. Shakhtshneider, E. V. Orlov, P. S. Malakhina, E. S. Voevoda, M. I. |
author_sort | Ovsyannikova, A. K. |
collection | PubMed |
description | Diabetes mellitus with autosomal dominant inheritance, i.e., maturity-onset diabetes of the young (MODY), is a genetic form of diabetes mellitus. The MODY phenotype is associated with gene mutations leading to pancreatic β-cell dysfunction. Here, we present the clinical case of a 50-year-old proband with familial diabetes mellitus in five generations (proband, her mother, grandmother, great-grandfather, and son). This disease is most likely associated with the novel Ser6Arg mutation in the HNF1A gene, which was identified in four family members. The mutation was not detected in MODY patients (126 subjects), in patients with type 2 diabetes mellitus (188 subjects), and in a general population sample (564 subjects). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13300-017-0350-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5801236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-58012362018-02-12 A Case of Maturity Onset Diabetes of the Young (MODY3) in a Family with a Novel HNF1A Gene Mutation in Five Generations Ovsyannikova, A. K. Rymar, O. D. Ivanoshchuk, D. E. Mikhailova, Svetlana V. Shakhtshneider, E. V. Orlov, P. S. Malakhina, E. S. Voevoda, M. I. Diabetes Ther Case Report Diabetes mellitus with autosomal dominant inheritance, i.e., maturity-onset diabetes of the young (MODY), is a genetic form of diabetes mellitus. The MODY phenotype is associated with gene mutations leading to pancreatic β-cell dysfunction. Here, we present the clinical case of a 50-year-old proband with familial diabetes mellitus in five generations (proband, her mother, grandmother, great-grandfather, and son). This disease is most likely associated with the novel Ser6Arg mutation in the HNF1A gene, which was identified in four family members. The mutation was not detected in MODY patients (126 subjects), in patients with type 2 diabetes mellitus (188 subjects), and in a general population sample (564 subjects). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13300-017-0350-8) contains supplementary material, which is available to authorized users. Springer Healthcare 2017-12-08 2018-02 /pmc/articles/PMC5801236/ /pubmed/29222740 http://dx.doi.org/10.1007/s13300-017-0350-8 Text en © The Author(s) 2017 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Case Report Ovsyannikova, A. K. Rymar, O. D. Ivanoshchuk, D. E. Mikhailova, Svetlana V. Shakhtshneider, E. V. Orlov, P. S. Malakhina, E. S. Voevoda, M. I. A Case of Maturity Onset Diabetes of the Young (MODY3) in a Family with a Novel HNF1A Gene Mutation in Five Generations |
title | A Case of Maturity Onset Diabetes of the Young (MODY3) in a Family with a Novel HNF1A Gene Mutation in Five Generations |
title_full | A Case of Maturity Onset Diabetes of the Young (MODY3) in a Family with a Novel HNF1A Gene Mutation in Five Generations |
title_fullStr | A Case of Maturity Onset Diabetes of the Young (MODY3) in a Family with a Novel HNF1A Gene Mutation in Five Generations |
title_full_unstemmed | A Case of Maturity Onset Diabetes of the Young (MODY3) in a Family with a Novel HNF1A Gene Mutation in Five Generations |
title_short | A Case of Maturity Onset Diabetes of the Young (MODY3) in a Family with a Novel HNF1A Gene Mutation in Five Generations |
title_sort | case of maturity onset diabetes of the young (mody3) in a family with a novel hnf1a gene mutation in five generations |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801236/ https://www.ncbi.nlm.nih.gov/pubmed/29222740 http://dx.doi.org/10.1007/s13300-017-0350-8 |
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