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Up to: Inherited retinal dystrophy · Retinal vascular disorder · Type 1 interferonopathy of childhood · TREX1-related type 1 interferonopathy

Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations

An inherited group of small vessel diseases comprised of cerebroretinal vasculopathy (CRV), hereditary vascular retinopathy (HRV) and hereditary endotheliopathy with retinopathy, nephropathy and stroke (HERNS); all exhibiting progressive visual impairment as well as variable cerebral dysfunction.

3 trials tagged with this condition →

This condition has no sub-types.