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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Landau-Kleffner syndrome
Epileptic encephalopathy with continuous spike-and-wave during sleep

GRIN2A GRIN2A


COMMON
GENES
GRIN2A



Citations in the biomedical literature:


Landau-Kleffner syndrome
GRIN2A
Epileptic encephalopathy with continuous spike-and-wave during sleep



Landau-Kleffner syndrome
Epileptic encephalopathy with continuous spike-and-wave during sleep

Synonym(s):
(no synonyms)

Synonym(s):
- CSWSS syndrome
- ESES
- Electrical status epilepticus during slow sleep

Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Mental and behavioural disorders -

Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: any age
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: any age
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D018887
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.