Schwartz–Jampel syndrome is not related to malignant hyperthermia

Schwartz–Jampel syndrome (SJS) is a rare syndrome that is clinically characterized by myotonia and skeletal abnormalities. Most reports regarding SJS have stated that patients with SJS are susceptible to malignant hyperthermia (MH). The statement is incorrect. There is no report showing that SJS is...

Descripción completa

Detalles Bibliográficos
Autor principal: Godai, Kohei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804619/
https://www.ncbi.nlm.nih.gov/pubmed/29457076
http://dx.doi.org/10.1186/s40981-017-0104-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804619/
https://www.ncbi.nlm.nih.gov/pubmed/29457076
http://dx.doi.org/10.1186/s40981-017-0104-7

Ejemplares similares