Journal of Pediatric Neurosciences
CASE REPORT
Year
: 2016  |  Volume : 11  |  Issue : 3  |  Page : 255--257

Schwartz–Jampel syndrome with gastroduodenal bleeding


Ipek Polat, Pakize Karaoğlu, UluÁ Yis, Semra Hiz Kurul 
 Department of Pediatrics, Division of Child Neurology, School of Medicine, Dokuz Eylul University, Izmir, Turkey

Correspondence Address:
Ipek Polat
Department of Pediatrics, Division of Child Neurology, School of Medicine, Dokuz Eylul University, Izmir
Turkey

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.


How to cite this article:
Polat I, Karaoğlu P, Yis U, Kurul SH. Schwartz–Jampel syndrome with gastroduodenal bleeding.J Pediatr Neurosci 2016;11:255-257


How to cite this URL:
Polat I, Karaoğlu P, Yis U, Kurul SH. Schwartz–Jampel syndrome with gastroduodenal bleeding. J Pediatr Neurosci [serial online] 2016 [cited 2021 May 13 ];11:255-257
Available from: https://www.pediatricneurosciences.com/article.asp?issn=1817-1745;year=2016;volume=11;issue=3;spage=255;epage=257;aulast=Polat;type=0