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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Detalles Bibliográficos
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:
Case Report
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

Internet

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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