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Cerebroretinal vasculopathy

1 OMIM reference -
1 associated gene
10 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 2

Hereditary vascular retinopathy

1 OMIM reference -
1 associated gene
3 signs/symptoms

Cerebroretinal vasculopathy

Hereditary vascular retinopathy

TREX1

(UniProt - OMIM)

(UniProt - OMIM)


COMMON GENES	TREX1

Citations in the biomedical literature:

Cerebroretinal vasculopathy		Hereditary vascular retinopathy
	Synonym(s): - CRV - Grand-Kaine-Fulling syndrome		Synonym(s): - HVR - Hereditary vascular retinopathy - Raynaud phenomenon - migraine

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

	Classification (ICD10): (no data available)		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - 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: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references


COMMON SIGNS	- Autosomal dominant inheritance - Visual loss / blindness / amblyopia

Cerebroretinal vasculopathy		Hereditary vascular retinopathy
	Very frequent - Mild visual loss / impaired visual acuity - Retinal vascular anomalies / retinal telangiectasia - Structural anomalies of the nervous system Frequent - Hemiplegia / diplegia / hemiparesia / limb palsy - Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia Occasional - Cataract / lens opacification - Glaucoma - Seizures / epilepsy / absences / spasms / status epilepticus		Very frequent - Anomalies of eyes and vision