Familial Cortical Myoclonic Tremor and Epilepsy, an Enigmatic Disorder: From Phenotypes to Pathophysiology and Genetics. A Systematic Review

BACKGROUND: Autosomal dominant familial cortical myoclonic tremor and epilepsy (FCMTE) is characterized by distal tremulous myoclonus, generalized seizures, and signs of cortical reflex myoclonus. FCMTE has been described in over 100 pedigrees worldwide, under several different names and acronyms. P...

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Detalles Bibliográficos
Autores principales: van den Ende, Tom, Sharifi, Sarvi, van der Salm, Sandra M. A., van Rootselaar, Anne-Fleur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Columbia University Libraries/Information Services 2018
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801339/
https://www.ncbi.nlm.nih.gov/pubmed/29416935
http://dx.doi.org/10.7916/D85155WJ

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801339/
https://www.ncbi.nlm.nih.gov/pubmed/29416935
http://dx.doi.org/10.7916/D85155WJ

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