Descriptor English: | Landau-Kleffner Syndrome | ||||||
Descriptor Spanish: |
Síndrome de Landau-Kleffner
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Descriptor Portuguese: | Síndrome de Landau-Kleffner | ||||||
Descriptor French: | Syndrome de Landau-Kleffner | ||||||
Entry term(s): |
Acquired Aphasia with Convulsive Disorder Acquired Childhoood Aphasia with Convulsive Disorder Acquired Epileptic Aphasia Acquired Epileptic Aphasias Acquired Epileptiform Aphasia Acquired Epileptiform Aphasias Aphasia, Acquired Epileptic Aphasia, Acquired, With Convulsive Disorder Aphasia, Epileptic, Acquired Epileptic Aphasia, Acquired Epileptic Aphasias, Acquired Epileptiform Aphasia, Acquired Epileptiform Aphasias, Acquired Landau Kleffner Acquired Epileptiform Aphasia Landau Kleffner Syndrome Landau-Kleffner Acquired Epileptiform Aphasia Syndrome, Landau-Kleffner |
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Tree number(s): |
C10.228.140.490.493.500 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D018887 | ||||||
Scope note: | 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). |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Previous Indexing: |
Aphasia (1982-1995) Epilepsy (1982-1995) |
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Public MeSH Note: | 1996 |
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History Note: | 1996 |
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Related: |
Aphasia
MeSH | ||||||
DeCS ID: | 32703 | ||||||
Unique ID: | D018887 | ||||||
NLM Classification: | WL 340.5 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 1996/01/01 | ||||||
Date of Entry: | 1994/12/27 | ||||||
Revision Date: | 2017/02/24 |
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Landau-Kleffner Syndrome
- Preferred
Concept UI |
M0028246 |
Scope note | 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). |
Preferred term | Landau-Kleffner Syndrome |
Entry term(s) |
Acquired Aphasia with Convulsive Disorder Acquired Childhoood Aphasia with Convulsive Disorder Acquired Epileptic Aphasia Acquired Epileptic Aphasias Acquired Epileptiform Aphasia Acquired Epileptiform Aphasias Aphasia, Acquired Epileptic Aphasia, Acquired, With Convulsive Disorder Aphasia, Epileptic, Acquired Epileptic Aphasia, Acquired Epileptic Aphasias, Acquired Epileptiform Aphasia, Acquired Epileptiform Aphasias, Acquired Landau Kleffner Acquired Epileptiform Aphasia Landau Kleffner Syndrome Landau-Kleffner Acquired Epileptiform Aphasia Syndrome, Landau-Kleffner |
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