Epilepsy syndrome adolescence adult onset type

General Details:

Name:
Epilepsy syndrome adolescence adult onset type
Steward:
NINDS
Definition:
Common epilepsy syndromes for adolescents, children 12-18 years of age, and adults, person older than 18 years of age.
Registration Status:
Qualified

Permissible Values:

Data Type:
Value List
Unit of Measure:
Ids:
Value Code Name Code Code System Code Description
Juvenile absence epilepsy Juvenile absence epilepsy Juvenile absence epilepsy (JAE)
Juvenile myoclonic epilepsy Juvenile myoclonic epilepsy Juvenile myoclonic epilepsy (JME)
Progressive myoclonus epilepsies Progressive myoclonus epilepsies Progressive myoclonus epilepsies (PME)
Autosomal Dominant Epilepsy with Auditory Features Autosomal Dominant Epilepsy with Auditory Features Autosomal Dominant Epilepsy with Auditory Features (ADEAF)
Other familial temporal lobe epilepsies Other familial temporal lobe epilepsies Other familial temporal lobe epilepsies
Epilepsy with generalized tonic-clonic seizures alone Epilepsy with generalized tonic-clonic seizures alone Epilepsy with generalized tonic-clonic seizures alone
Other, specify Other, specify Other, specify

Designations:

Designation:
Epilepsy syndrome adolescence adult onset type
Tags:

Designations:

Definition:
Common epilepsy syndromes for adolescents, children 12-18 years of age, and adults, person older than 18 years of age.
Tags:

Reference Documents:

ID:
Title:
URI:
Provider Org:
Language Code:
Document:
EPILEPSY: Berg AT, Berkovic SF, Brodie MJ, Buchhalter J, et al. Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009. Epilepsia. 2010 Apr;51(4):676-85. http://www.ilae-epilepsy.org/Visitors/Centre/ctf/ctfoverview.cfm

Identifiers:

Source:
NLM
Id:
ST62StcHRCH
Version:
3.1
Source:
NINDS
Id:
C14477
Version:
3
Source:
BRICS Variable Name
Id:
EpilepsySyndAdolAdltOnsTyp
Version: