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2 OMIM references -
6 associated genes
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
4 signs/symptoms
West syndrome
Spasticity - intellectual deficit - X-linked epilepsy

ARX ARX
CDKL5
GRIN2B
PIGA
SCN2A
ST3GAL3


COMMON
GENES
ARX



Citations in the biomedical literature:


West syndrome
ARX CDKL5 GRIN2B PIGA SCN2A ST3GAL3

Spasticity - intellectual deficit - X-linked epilepsy



West syndrome
Spasticity - intellectual deficit - X-linked epilepsy

Synonym(s):
- Infantile spasms
- Intellectual deficit - hypsarrhythmia

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: no data available
Average age of death: -
Type of inheritance: x-linked recessive

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

Spasticity - intellectual deficit - X-linked epilepsy

Very frequent
- Hemiplegia / diplegia / hemiparesia / limb palsy
- Hypertonia / spasticity / rigidity / stiffness
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Seizures / epilepsy / absences / spasms / status epilepticus



West syndrome

(no data available)