Morvan syndrome

Morvan syndrome is a rare, life-threatening, acquired neurologic disease characterized by neuromyotonia, dysautonomia and encephalopathy with severe insomnia. Signs involving central (e.g. hallucinations, confusion, amnesia, myoclonus), autonomic (e.g. variations in blood pressure, hyperhidrosis) and peripheral (e.g. painful cramps, myokymia) hyperactivity, as well as systemic manifestations (such as weight loss, pruritus, fever), are reported. Thymoma is present in some cases.

Also known as: Morvan's fibrillary chorea, limbic encephalitis-neuromyotonia-hyperhidrosis-polyneuropathy syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Morvan syndrome itself.