Published in:
01-12-2017 | Letter to the Editor
Wilson’s disease presenting as central pontine myelinolysis
Authors:
Mahdi Safdarian, Renato P. Munhoz, Mahboubeh Aghaei, Mohammad Rohani
Published in:
Neurological Sciences
|
Issue 12/2017
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Excerpt
Wilson’s disease (WD) is a rare autosomal recessive disease due to impaired biliary excretion of copper. Its main neurologic symptoms are dysarthria and movement disorders such as dystonia, tremor, and parkinsonism [
1,
2]. Herein, we report a case of central pontine myelinolysis (CPM) presenting as an uncommon presentation of WD. …