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A Case of Fulminant Type 1 Diabetes with Gastric and Urinary Retention

Fulminant type 1 diabetes (fT1D) is a severe subtype of type 1 diabetes which progresses rapidly with islet cells destroyed almost completely within a short period of time. It is often characterized by flu-like or gastrointestinal symptoms at the onset with negative islet-associated autoantibodies,...

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Detalles Bibliográficos
Autores principales: Xing, Chuan, Zhao, Wenqian, Wang, Yanjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349281/
https://www.ncbi.nlm.nih.gov/pubmed/30460498
http://dx.doi.org/10.1007/s13300-018-0533-y
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author Xing, Chuan
Zhao, Wenqian
Wang, Yanjun
author_facet Xing, Chuan
Zhao, Wenqian
Wang, Yanjun
author_sort Xing, Chuan
collection PubMed
description Fulminant type 1 diabetes (fT1D) is a severe subtype of type 1 diabetes which progresses rapidly with islet cells destroyed almost completely within a short period of time. It is often characterized by flu-like or gastrointestinal symptoms at the onset with negative islet-associated autoantibodies, resulting in an absolute deficiency of endogenous insulin secretion. Poor prognosis can be caused by the significantly higher incidence of metabolic disorders (such as severe ion disorders and elevated serum pancreatic enzymes), acute and chronic complications if not diagnosed and treated in a timely manner. We herein describe an fT1D patient with gastric and urinary retention along with severe ion disturbance, whose laboratory tests revealed diabetic ketoacidosis, peripheral neuropathy, retinopathy, nephropathy, and hypoproteinemia.
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spelling pubmed-63492812019-02-15 A Case of Fulminant Type 1 Diabetes with Gastric and Urinary Retention Xing, Chuan Zhao, Wenqian Wang, Yanjun Diabetes Ther Case Report Fulminant type 1 diabetes (fT1D) is a severe subtype of type 1 diabetes which progresses rapidly with islet cells destroyed almost completely within a short period of time. It is often characterized by flu-like or gastrointestinal symptoms at the onset with negative islet-associated autoantibodies, resulting in an absolute deficiency of endogenous insulin secretion. Poor prognosis can be caused by the significantly higher incidence of metabolic disorders (such as severe ion disorders and elevated serum pancreatic enzymes), acute and chronic complications if not diagnosed and treated in a timely manner. We herein describe an fT1D patient with gastric and urinary retention along with severe ion disturbance, whose laboratory tests revealed diabetic ketoacidosis, peripheral neuropathy, retinopathy, nephropathy, and hypoproteinemia. Springer Healthcare 2018-11-20 2019-02 /pmc/articles/PMC6349281/ /pubmed/30460498 http://dx.doi.org/10.1007/s13300-018-0533-y Text en © The Author(s) 2018 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
Xing, Chuan
Zhao, Wenqian
Wang, Yanjun
A Case of Fulminant Type 1 Diabetes with Gastric and Urinary Retention
title A Case of Fulminant Type 1 Diabetes with Gastric and Urinary Retention
title_full A Case of Fulminant Type 1 Diabetes with Gastric and Urinary Retention
title_fullStr A Case of Fulminant Type 1 Diabetes with Gastric and Urinary Retention
title_full_unstemmed A Case of Fulminant Type 1 Diabetes with Gastric and Urinary Retention
title_short A Case of Fulminant Type 1 Diabetes with Gastric and Urinary Retention
title_sort case of fulminant type 1 diabetes with gastric and urinary retention
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349281/
https://www.ncbi.nlm.nih.gov/pubmed/30460498
http://dx.doi.org/10.1007/s13300-018-0533-y
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