Retinal vasculopathy and cerebral leukodystrophy (Q41772): Difference between revisions
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Vasculopatia retiniana e leucodistrofia cerebral são um grupo hereditário de doenças de pequenos vasos compostas por vasculopatia cerebrorretiniana, retinopatia vascular hereditária e endoteliopatia hereditária com retinopatia, nefropatia e acidente vascular cerebral (HERNS); todos exibindo comprometimento visual progressivo, bem como disfunção cerebral variável. | |||
| description / en | description / en | ||
Retinal vasculopathy and cerebral leukodystrophy is an inherited group of small vessel diseases comprised of cerebroretinal vasculopathy, hereditary vascular retinopathy and hereditary endotheliopathy with retinopathy, nephropathy and stroke (HERNS); all exhibiting progressive visual impairment as well as variable cerebral dysfunction. | |||
Revision as of 08:03, 13 August 2026
Retinal vasculopathy and cerebral leukodystrophy is an inherited group of small vessel diseases comprised of cerebroretinal vasculopathy, hereditary vascular retinopathy and hereditary endotheliopathy with retinopathy, nephropathy and stroke (HERNS); all exhibiting progressive visual impairment as well as variable cerebral dysfunction.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 9B78.0 |
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| English | Retinal vasculopathy and cerebral leukodystrophy |
Retinal vasculopathy and cerebral leukodystrophy is an inherited group of small vessel diseases comprised of cerebroretinal vasculopathy, hereditary vascular retinopathy and hereditary endotheliopathy with retinopathy, nephropathy and stroke (HERNS); all exhibiting progressive visual impairment as well as variable cerebral dysfunction. |
