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Juvenile Myoclonic Epilepsy Presenting with Neurocognitive Impairment: A Case Report

Juvenile myoclonic epilepsy (JME) is a genetically and clinically diverse disorder which is characterized by myoclonic jerks, usually after awakening from sleep. It affects both genders equally and manifests during the second decade of life. The various precipitating factors include stress, light, s...

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Detalles Bibliográficos
Autores principales: Mahesar, Sarfraz, Akbar, Hira F, Abid, Husnain, Sana, Rabia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5935437/
https://www.ncbi.nlm.nih.gov/pubmed/29736355
http://dx.doi.org/10.7759/cureus.2271