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Aicardi-GoutiÃ¨res syndrome

7 OMIM references -
6 associated genes
10 signs/symptoms

COMMON GENES: 1

Hereditary vascular retinopathy

1 OMIM reference -
1 associated gene
3 signs/symptoms

Aicardi-GoutiÃ¨res syndrome

Hereditary vascular retinopathy

ADAR	(UniProt - OMIM)		TREX1	(UniProt - OMIM)
RNASEH2A	(UniProt - OMIM)
RNASEH2B	(UniProt - OMIM)
RNASEH2C	(UniProt - OMIM)
SAMHD1	(UniProt - OMIM)
TREX1	(UniProt - OMIM)


COMMON GENES	TREX1

Citations in the biomedical literature:

Aicardi-GoutiÃ¨res syndrome		Hereditary vascular retinopathy
	Synonym(s): - Encephalopathy with basal ganglia calcification - Encephalopathy with intracranial calcification and chronic lymphocytosis of cerebrospinal fluid		Synonym(s): - HVR - Hereditary vascular retinopathy - Raynaud phenomenon - migraine

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: child / adolescent Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: no data available Type of inheritance: autosomal dominant

	External references: 7 OMIM references - 1 MeSH reference: C535607		External references: 1 OMIM reference - No MeSH references

Aicardi-GoutiÃ¨res syndrome		Hereditary vascular retinopathy
	Very frequent - Holoprosencephaly / arhinencephaly / unique lateral ventricle - Hypertonia / spasticity / rigidity / stiffness - Intellectual deficit / mental / psychomotor retardation / learning disability - Porencephaly Frequent - Coloboma of the eyelid - Hemiplegia / diplegia / hemiparesia / limb palsy Occasional - Microcephaly - Plagiocephaly - Ptosis - Seizures / epilepsy / absences / spasms / status epilepticus		Very frequent - Anomalies of eyes and vision - Autosomal dominant inheritance - Visual loss / blindness / amblyopia