FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.7  |  FHIR Version n/a  User: [n/a]

230438007: Landau-Kleffner syndrome (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
345312010 Acquired epileptic aphasia en Synonym (core metadata concept) Inactive Entire term case insensitive (core metadata concept) SNOMED CT core
345313017 Landau-Kleffner syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
618245014 Acquired epileptic aphasia (disorder) en Fully specified name Inactive Entire term case insensitive (core metadata concept) SNOMED CT core
2951784017 Acquired aphasia with epilepsy en Synonym (core metadata concept) Inactive Entire term case insensitive (core metadata concept) SNOMED CT core
3683660018 Aphasia co-occurrent with epilepsy en Synonym (core metadata concept) Inactive Entire term case insensitive (core metadata concept) SNOMED CT core
5373709014 Landau-Kleffner syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
5373710016 LKS - Landau-Kleffner syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5464927011 A type of EE-SWAS that presents in individuals with normal development and cognition. It is characterised by plateauing or regression of language, with an acquired agnosia that is concomitant with significant activation of spike-and-wave complexes during sleep. Onset of epileptic seizures is between 2 and 12 years of age. Epileptic seizures may or may not be clinically evident. There is no mandatory seizure type although focal seizures are common. Neurological examination is normal. The EEG background during wakefulness may show focal or diffuse slowing and often contains focal or multifocal abnormalities but may be normal. Epileptiform abnormalities during wakefulness are not continuous. In drowsiness and sleep, there is marked activation of epileptiform activity, with slow (1.5 - 2Hz) spike-and-wave complexes in N-REM sleep. Spike-and-wave activation in sleep (SWAS) is usually diffuse but may occur more focally or multifocally. Normal sleep architecture is absent or difficult to distinguish. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5464928018 A type of EE-SWAS that presents in individuals with normal development and cognition. It is characterized by plateauing or regression of language, with an acquired agnosia that is concomitant with significant activation of spike-and-wave complexes during sleep. Onset of epileptic seizures is between 2 and 12 years of age. Epileptic seizures may or may not be clinically evident. There is no mandatory seizure type although focal seizures are common. Neurological examination is normal. The EEG background during wakefulness may show focal or diffuse slowing and often contains focal or multifocal abnormalities but may be normal. Epileptiform abnormalities during wakefulness are not continuous. In drowsiness and sleep, there is marked activation of epileptiform activity, with slow (1.5 - 2Hz) spike-and-wave complexes in N-REM sleep. Spike-and-wave activation in sleep (SWAS) is usually diffuse but may occur more focally or multifocally. Normal sleep architecture is absent or difficult to distinguish. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Landau-Kleffner syndrome Is a Disorder of speech and language development false Inferred relationship Some
Landau-Kleffner syndrome Finding site Brain structure false Inferred relationship Some
Landau-Kleffner syndrome Is a Aphasia false Inferred relationship Some
Landau-Kleffner syndrome Finding site Cerebrum true Inferred relationship Some 1
Landau-Kleffner syndrome Due to Epilepsy false Inferred relationship Some 2
Landau-Kleffner syndrome Is a Epilepsy false Inferred relationship Some
Landau-Kleffner syndrome Is a Childhood seizure false Inferred relationship Some
Landau-Kleffner syndrome Is a Central nervous system complication false Inferred relationship Some
Landau-Kleffner syndrome Occurrence Childhood true Inferred relationship Some 1
Landau-Kleffner syndrome Has interpretation Abnormal true Inferred relationship Some 3
Landau-Kleffner syndrome Interprets Ability to perform functions related to communication true Inferred relationship Some 3
Landau-Kleffner syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Landau-Kleffner syndrome Interprets Speech and language observable false Inferred relationship Some 4
Landau-Kleffner syndrome Is a Acquired language disorder true Inferred relationship Some
Landau-Kleffner syndrome Is a Epileptic encephalopathy with spike-and-wave activation in sleep true Inferred relationship Some
Landau-Kleffner syndrome Is a Developmental aphasia true Inferred relationship Some
Landau-Kleffner syndrome Finding site Brain structure true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start