Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease gaucher disease
Symptom C0027066|myoclonus
Sentences 2
PubMedID- 20004867 The n188s mutation in gaucher disease is associated with myoclonus epilepsy.
PubMedID- 22569507 We present the first reported case of a rapid clinical and electroencephalographic response to intravenous levetiracetam infusion of myoclonic status epilepticus in a patient with progressive myoclonus epilepsy due to gaucher disease.

Page: 1