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Hereditary vascular retinopathy

Orpha number ORPHA71291
Synonym(s) HVR
Hereditary vascular retinopathy - Raynaud phenomenon - migraine
Prevalence <1 / 1 000 000
Inheritance Autosomal dominant
Age of onset Adult
ICD-10 -
ICD-O -
OMIM
UMLS -
MeSH -
MedDRA -

Summary

Hereditary vascular retinopathy (HVR) is a phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leukodystrophy (RVCL; see this term) and characterized by progressive visual impairment, strokes and often associated with Raynaud phenomenon and migraine-like symptoms.


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Detailed information

Article for general public
  • DE (2013,pdf)
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