Epilepsy, Focal, with Speech Disorder and with or Without Impaired Intellectual Development (FESD)

Alias:

Continuous Spike and Waves During Slow-Wave Sleep Syndrome

Landau-Kleffner Syndrome

Early-Onset Epileptic Encephalopathy and Intellectual Disability Due to Grin2a Mutation

Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation

Fesd

Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, Autosomal Dominant

Epilepsy, Focal, with Speech Disorder with/without Mental Retardation

Benign Epilepsy of Childhood with Centrotemporal Spikes

Aphasia, Acquired, with Epilepsy

Acquired Aphasia with Epilepsy

Benign Rolandic Epilepsy

Aphasia

Adresd

Resdad

Bects

Cswss

Csws

Lks

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Epilepsy, Focal, with Speech Disorder and with or Without Impaired Intellectual Development, also known as continuous spike and waves during slow-wave sleep syndrome, is related to centralopathic epilepsy and benign epilepsy with centrotemporal spikes, and has symptoms including back pain, cachexia and cyanosis. An important gene associated with Epilepsy, Focal, with Speech Disorder and with or Without Impaired Intellectual Development is GRIN2A (Glutamate Ionotropic Receptor NMDA Type Subunit 2A). The drugs Levetiracetam and Memantine have been mentioned in the context of this disorder. Affiliated tissues include temporal lobe and brain, and related phenotypes are intellectual disability, severe and specific learning disability

Related ID：

MALACARDS：EPL258

OMIM：245570

MESH：D001037