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A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia
We describe the case of a six year old boy with findings consistent with myotonia congenita: muscular hypertrophy, stiffness when commencing movements and typical warm-up signs. The most prominent symptom was myotonia of the eyelid muscles with apparent swelling around the eyes. Even though the pron...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240542/ https://www.ncbi.nlm.nih.gov/pubmed/27858731 http://dx.doi.org/10.3233/JND-150069 |