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Published in 2017 at "Neurology"
DOI: 10.1212/wnl.0000000000003507
Abstract: Sturge-Weber syndrome is a rare, sporadic, neurocutaneous disorder classically characterized by a facial nevus in the trigeminal distribution (port wine stain), leptomeningeal angiomatosis, and glaucoma, although intracranial changes can be present without cutaneous involvement.1 Seizures…
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Keywords:
cricopharyngeal dystonia;
ten year;
stimulation cricopharyngeal;
pallidal stimulation ... See more keywords