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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...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Veröffentlicht in:Cureus
Hauptverfasser: Mahesar, Sarfraz, Akbar, Hira F, Abid, Husnain, Sana, Rabia
Format: Artigo
Sprache:Inglês
Veröffentlicht: Cureus 2018
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5935437/
https://ncbi.nlm.nih.gov/pubmed/29736355
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.2271
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