ABSTRACT
West's syndrome is an age-specific set of symptoms consisting of myoclonic epilepsy (infantile spasms), an interictal electroencephalographic pattern (hypsarrhythmia), and moderate-to-severe mental retardation. Infantile spasms were first reported in 1841, but all three characteristics were not described until 1951. The basic pathophysiology of and ideal therapy for the seizures remain undefined. The author reviews the historical aspects, clinical manifestations, etiology, diagnostic evaluation, and treatment of West's syndrome.
- Received October 1983.
- Accepted October 1983.
- Copyright © 1984 The Cleveland Clinic Foundation. All Rights Reserved.
Log in using your username and password
Registration is Now Required for Free Access to CCJM Content
Register once and log in for full access to articles and content. Click “Register” in the upper right corner and follow the simple instructions to create a new account.
If you are using a mobile device, click on the settings icon to access the Register link.
Jump to section
Related Articles
Cited By...
- No citing articles found.