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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...

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Autores principales: Polat, İpek, Karaoğlu, Pakize, Yiş, Uluç, Kurul, Semra Hız
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
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.
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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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