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Steinert's syndrome presenting as anal incontinence: a case report
INTRODUCTION: Myotonic dystrophy (MD) or Steinert's syndrome is a rare cause of chronic diarrhea and anal incontinence. In the presence of chronic diarrhea and fecal incontinence with muscle weakness, neuromuscular disorders such as myotonic dystrophy should be considered in the differential di...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170350/ https://www.ncbi.nlm.nih.gov/pubmed/21838873 http://dx.doi.org/10.1186/1752-1947-5-371 |
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author | Erdenen, Fusun Toros, Ahmet Burak Uzum, Ayse Kubat Sacak, Sirin |
author_facet | Erdenen, Fusun Toros, Ahmet Burak Uzum, Ayse Kubat Sacak, Sirin |
author_sort | Erdenen, Fusun |
collection | PubMed |
description | INTRODUCTION: Myotonic dystrophy (MD) or Steinert's syndrome is a rare cause of chronic diarrhea and anal incontinence. In the presence of chronic diarrhea and fecal incontinence with muscle weakness, neuromuscular disorders such as myotonic dystrophy should be considered in the differential diagnosis. CASE PRESENTATION: We present the case of a 45-year-old Turkish man with Steinert's syndrome, who was not diagnosed until the age of 45. CONCLUSIONS: In clinical practice, the persistence of diarrhea and fecal incontinence with muscle weakness should suggest that the physician perform an anal manometric study and electromyography. Neuromuscular disorders such as myotonic dystrophy should be considered in the differential diagnosis. |
format | Online Article Text |
id | pubmed-3170350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31703502011-09-10 Steinert's syndrome presenting as anal incontinence: a case report Erdenen, Fusun Toros, Ahmet Burak Uzum, Ayse Kubat Sacak, Sirin J Med Case Reports Case Report INTRODUCTION: Myotonic dystrophy (MD) or Steinert's syndrome is a rare cause of chronic diarrhea and anal incontinence. In the presence of chronic diarrhea and fecal incontinence with muscle weakness, neuromuscular disorders such as myotonic dystrophy should be considered in the differential diagnosis. CASE PRESENTATION: We present the case of a 45-year-old Turkish man with Steinert's syndrome, who was not diagnosed until the age of 45. CONCLUSIONS: In clinical practice, the persistence of diarrhea and fecal incontinence with muscle weakness should suggest that the physician perform an anal manometric study and electromyography. Neuromuscular disorders such as myotonic dystrophy should be considered in the differential diagnosis. BioMed Central 2011-08-12 /pmc/articles/PMC3170350/ /pubmed/21838873 http://dx.doi.org/10.1186/1752-1947-5-371 Text en Copyright ©2011 Erdenen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Erdenen, Fusun Toros, Ahmet Burak Uzum, Ayse Kubat Sacak, Sirin Steinert's syndrome presenting as anal incontinence: a case report |
title | Steinert's syndrome presenting as anal incontinence: a case report |
title_full | Steinert's syndrome presenting as anal incontinence: a case report |
title_fullStr | Steinert's syndrome presenting as anal incontinence: a case report |
title_full_unstemmed | Steinert's syndrome presenting as anal incontinence: a case report |
title_short | Steinert's syndrome presenting as anal incontinence: a case report |
title_sort | steinert's syndrome presenting as anal incontinence: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170350/ https://www.ncbi.nlm.nih.gov/pubmed/21838873 http://dx.doi.org/10.1186/1752-1947-5-371 |
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