Differences
This shows you the differences between two versions of the page.
Both sides previous revision Previous revision | Next revisionBoth sides next revision | ||
content:lennox-gastaut_syndrome [2020/02/04 14:27] – biju.hameed@gmail.com | content:lennox-gastaut_syndrome [2020/02/08 13:35] – bijuhameed | ||
---|---|---|---|
Line 1: | Line 1: | ||
====== Lennox-Gastaut syndrome ====== | ====== Lennox-Gastaut syndrome ====== | ||
- | + | {[page> | |
<alert type=" | <alert type=" | ||
Lennox-Gastaut syndrome (LGS) is an epileptic encephalopathy and is defined by a triad of multiple drug-resistant seizure types, a specific EEG pattern showing bursts of slow spike-wave complexes or generalized paroxysmal fast activity, and intellectual disability. The prevalence of LGS is estimated between 1 and 2% of all patients with epilepsy. | Lennox-Gastaut syndrome (LGS) is an epileptic encephalopathy and is defined by a triad of multiple drug-resistant seizure types, a specific EEG pattern showing bursts of slow spike-wave complexes or generalized paroxysmal fast activity, and intellectual disability. The prevalence of LGS is estimated between 1 and 2% of all patients with epilepsy. |