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Schwartz–Jampel syndrome with gastroduodenal bleeding
Schwartz–Jampel syndrome is a rare autosomal recessive disorder with joint contractures, generalized myotonia, skeletal anomalies, and facial dysmorphism. The patients with Schwartz–Jampel syndrome have muscle stiffness and electromyography reveals complex, repetitive discharges as myotonic discharg...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108135/ https://www.ncbi.nlm.nih.gov/pubmed/27857801 http://dx.doi.org/10.4103/1817-1745.193351 |
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author | Polat, İpek Karaoğlu, Pakize Yiş, Uluç Kurul, Semra Hız |
author_facet | Polat, İpek Karaoğlu, Pakize Yiş, Uluç Kurul, Semra Hız |
author_sort | Polat, İpek |
collection | PubMed |
description | Schwartz–Jampel syndrome is a rare autosomal recessive disorder with joint contractures, generalized myotonia, skeletal anomalies, and facial dysmorphism. The patients with Schwartz–Jampel syndrome have muscle stiffness and electromyography reveals complex, repetitive discharges as myotonic discharges. It is unusual for a Schwartz-Jampel syndrome case to have recurrent gastrointestinal bleeding episodes. The stable endothelial barrier is provided by perlecan which is an important component of vascular structures. Thus, perlecan deficiency may cause recurrent gastroduodenal bleeding. Our report is unique with being the first reported Schwartz–Jampel syndrome case with gastrointestinal bleeding. |
format | Online Article Text |
id | pubmed-5108135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51081352016-11-17 Schwartz–Jampel syndrome with gastroduodenal bleeding Polat, İpek Karaoğlu, Pakize Yiş, Uluç Kurul, Semra Hız J Pediatr Neurosci Case Report Schwartz–Jampel syndrome is a rare autosomal recessive disorder with joint contractures, generalized myotonia, skeletal anomalies, and facial dysmorphism. The patients with Schwartz–Jampel syndrome have muscle stiffness and electromyography reveals complex, repetitive discharges as myotonic discharges. It is unusual for a Schwartz-Jampel syndrome case to have recurrent gastrointestinal bleeding episodes. The stable endothelial barrier is provided by perlecan which is an important component of vascular structures. Thus, perlecan deficiency may cause recurrent gastroduodenal bleeding. Our report is unique with being the first reported Schwartz–Jampel syndrome case with gastrointestinal bleeding. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC5108135/ /pubmed/27857801 http://dx.doi.org/10.4103/1817-1745.193351 Text en Copyright: © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Polat, İpek Karaoğlu, Pakize Yiş, Uluç Kurul, Semra Hız Schwartz–Jampel syndrome with gastroduodenal bleeding |
title | Schwartz–Jampel syndrome with gastroduodenal bleeding |
title_full | Schwartz–Jampel syndrome with gastroduodenal bleeding |
title_fullStr | Schwartz–Jampel syndrome with gastroduodenal bleeding |
title_full_unstemmed | Schwartz–Jampel syndrome with gastroduodenal bleeding |
title_short | Schwartz–Jampel syndrome with gastroduodenal bleeding |
title_sort | schwartz–jampel syndrome with gastroduodenal bleeding |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108135/ https://www.ncbi.nlm.nih.gov/pubmed/27857801 http://dx.doi.org/10.4103/1817-1745.193351 |
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