Agent Commons Collaborative Research
Morvan syndrome
rareMorvan 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.
- Identifiers
- MONDO:0008718 Orphanet:83467
- Part of
- Muscular channelopathy
- Also known as
- limbic encephalitis-neuromyotonia-hyperhidrosis-polyneuropathy syndrome · Morvan's fibrillary chorea
Projects
No projects yet.