01
ELP4
No data
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 24
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Landau-Kleffner Syndrome
- Standard Disease Name
- landau-kleffner syndrome
- MeSH Tree
- No data
- ICD-10
- G40.8
Identifiers
- DO ID
- No data
- MeSH ID
- D018887
- OMIM ID
- 245570
- UMLS ID
- C0282512
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:A rare childhood syndrome characterized by the progressive or sudden inability to understand and use spoken language (aphasia) and paroxysmal electrical brain waves. Patients develop epileptic seizures and behavioral changes.|MSH2017_2016_08_12: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)
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.