- Lennox–
Gastaut syndrome (LGS) is a complex, rare, and
severe childhood-onset
epilepsy syndrome. It is
characterized by
multiple and
concurrent seizure...
-
Geschwind syndrome, also
known as
Gastaut–Geschwind syndrome, is a
group of
behavioral phenomena evident in some
people with
temporal lobe epilepsy. It...
-
Henri Jean
Pascal Gastaut (April 15, 1915,
Monaco – July 14, 1995 M****ille) was a
French neurologist and epileptologist.
Gastaut was
educated in medicine...
-
includes focal seizures, tonic-clonic seizures, and
seizures in Lennox-
Gastaut syndrome. In
bipolar disorder,
lamotrigine has not been
shown to reliably...
- in
absence epilepsy, but is
common in
several epilepsies such as Lennox-
Gastaut syndrome (LGS) and
Ohtahara syndrome.
Antiepileptic drugs (AEDs) are commonly...
- for the
treatment of
seizures ****ociated with
Dravet syndrome, Lennox–
Gastaut syndrome, or
tuberous sclerosis complex in
people one year of age and older...
- epilepsy, each
consisting of
focal seizures-
Gastaut and
Panayiotopoulos (Pan.).
Other names for the
Gastaut type
include benign epilepsy of
childhood with...
-
inhibitor being investigated as a
treatment for
Dravet syndrome, Lennox–
Gastaut syndrome,
tuberous sclerosis complex, dup15q syndrome, and CDKL5 deficiency...
- partial-onset seizures;
infantile spasm,
mixed seizure types of Lennox–
Gastaut syndrome,
myoclonic and
generalized tonic clonic seizure.
Despite this...
- used in
combination with
other medication and
therapy to
treat Lennox–
Gastaut syndrome and
various other seizure disorders. Rufinamide, a
triazole derivative...
