loading...| Preferred Name |
Landau-Kleffner Syndrome [Disease/Finding] |
|
| Synonyms |
Acquired Childhoood Aphasia with Convulsive Disorder |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003874 |
|
| altLabel |
Acquired Childhoood Aphasia with Convulsive Disorder Aphasia, Acquired, With Convulsive Disorder Acquired Aphasia with Convulsive Disorder Aphasia, Acquired Epileptic Aphasia, Epileptic, Acquired Landau-Kleffner Syndrome Landau-Kleffner Acquired Epileptiform Aphasia Acquired Epileptiform Aphasia |
|
| cui |
C0282512 |
|
| MESH 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. (From Menkes, Textbook of Child Neurology, 5th ed, pp749-50; J Child Neurol 1997 Nov;12(8):489-495) |
|
| MESH DUI |
D018887 |
|
| MeSH name |
Landau-Kleffner Syndrome |
|
| MESH UI |
M0028246 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000003874 |
|
| NUI |
N0000003874 |
|
| prefLabel |
Landau-Kleffner Syndrome [Disease/Finding] |
|
| SNOMED CID |
230438007 |
|
| tui |
T048 |
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| subClassOf |