A clinical and neurophysiological motor signature of Unverricht-Lundborg disease.

CONCLUSION: A homogeneous motor pattern was delineated that may represent a ULD clinical and neurophysiological signature. Clinical and neurophysiological findings confirmed the pure cortical origin of the permanent myoclonus. Also, oculomotor findings shed new light on ULD pathophysiology by evidencing combined midbrain and cerebellar dysfunction. PMID: 28688606 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/28688606?dopt=Abstract

Source: Revue Neurologique - July 11, 2017 Category: Neurology Tags: Rev Neurol (Paris) Source Type: research