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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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Formato: Artigo
Idioma:en
Publicado em: Medknow Publications & Media Pvt Ltd 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5108135/
https://ncbi.nlm.nih.gov/pubmed/27857801
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1817-1745.193351
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