别名 Cavarre disease、Familial Periodic Paralyses、Familial Periodic Paralysis + [42] |
简介 A heterogenous group of inherited disorders characterized by recurring attacks of rapidly progressive flaccid paralysis or myotonia. These conditions have in common a mutation of the gene encoding the alpha subunit of the sodium channel in skeletal muscle. They are frequently associated with fluctuations in serum potassium levels. Periodic paralysis may also occur as a non-familial process secondary to THYROTOXICOSIS and other conditions. (From Adams et al., Principles of Neurology, 6th ed, p1481) |
靶点 |
作用机制 CAs抑制剂 |
非在研适应症- |
最高研发阶段批准上市 |
首次获批国家/地区 美国 |
首次获批日期1958-07-22 |
开始日期2025-05-01 |
申办/合作机构 |
开始日期2019-10-01 |
申办/合作机构 |
开始日期2019-08-26 |
申办/合作机构 |
