Morvan综合征
Morvan syndrome
ORPHA:83467疾病
定义 英文原文(暂无中文)
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.
别名
边缘叶脑炎-神经性肌强直-多汗症-多发性神经病综合征
基本事实
- 发病年龄
- 成年期
- 患病率
- <1 / 1 000 000
临床表型 1
常见 79–30%1
- 抗CASPR2 HP:5000005
外部标识与链接
发现这一页有错误?告诉我 · 邮件主题会自动带上本页的 ORPHA 编号
本页数据来源
- 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
- 中文病名:Orphanet 中文包,冻结于 2020-06-01
- 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)