loading...| Preferred Name |
Landau-Kleffner Syndrome |
|
| Synonyms |
Landau-Kleffner Acquired Epileptiform Aphasia|Acquired Childhoood Aphasia with Convulsive Disorder|Acquired Epileptic Aphasia |
|
| ID |
http://bioontology.org/projects/ontologies/birnlex#birnlex_12747 |
|
| abbrev | ||
| class_or_indiv |
true |
|
| definition |
A syndrome characterized by the onset of isolated language dysfunction in otherwise normal children (age of onset 4-7 years) and epileptiform discharges on ELECTROENCEPHALOGRAPHY. Seizures, including atypical absence ( EPILEPSY, ABSENCE), complex partial ( EPILEPSY, COMPLEX PARTIAL), and other types may occur. The electroencephalographic abnormalities and seizures tend to resolve by puberty. The language disorder may also resolve although some individuals are left with severe language dysfunction, including APHASIA and auditory AGNOSIA (MeSH). |
|
| external_id_urls |
http://www.nlm.nih.gov/cgi/mesh/2008/MB_cgi?field=uid&term=D018887 |
|
| external_ids |
meshUID:D018887 |
|
| label |
Landau-Kleffner Syndrome |
|
| mod_date |
2007-10-08 |
|
| preferred_label |
Landau-Kleffner Syndrome |
|
| prefixIRI |
birnlex_12747 |
|
| retired |
false |
|
| synonyms |
Landau-Kleffner Acquired Epileptiform Aphasia|Acquired Childhoood Aphasia with Convulsive Disorder|Acquired Epileptic Aphasia |
|
| subClassOf |
http://bioontology.org/projects/ontologies/birnlex#birnlex_12718 |