Landau-Kleffner Syndrome (LKS)

Alias:
Acquired Epileptic Aphasia
Lks
Childhood Epileptic Aphasia
Landau Kleffner Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Landau-Kleffner Syndrome, also known as acquired epileptic aphasia, is related to auditory agnosia and verbal auditory agnosia. An important gene associated with Landau-Kleffner Syndrome is GRIN2A (Glutamate Ionotropic Receptor NMDA Type Subunit 2A), and among its related pathways/superpathways are Transmission across Chemical Synapses and Neuropathic Pain-Signaling in Dorsal Horn Neurons. The drugs Acetazolamide and Diazepam have been mentioned in the context of this disorder. Affiliated tissues include brain and temporal lobe, and related phenotypes are seizure and aphasia
Related ID:
MESH:D018887
ICD11:348544271

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Child
1-9/1000000
17
215
33

Medical Symptom

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Gene & Mutation

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Disease Model

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References Literature

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