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

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vasculopathie rétinienne avec leucoencéphalopathie cérébrale et manifestations systémiques

SNOMEDCT-CA (CRV), hereditary vascular retinopathy (HRV) and hereditary endotheliopathy with retinopathy, nephropathy and stroke all exhibiting progressive visual impairment as / 783787000

SNOMEDCT-CA (trouble) / 783787000

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pigmentary abnormality

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anomalie pigmentaire

IATE - Health

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pigmentary

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pigmentaire

IATE - Health

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A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are prenatal and postnatal growth delay, mild to severe intellectual disability, hemiatrophy, webbed neck, ocular and cutaneous pigmentary anomalies, cran

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trisomie 22 en mosaïque

SNOMEDCT-BE (disorder) / 764625002

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Others have searched : ataxia with pigmentary retinopathy grade i rop grade i retinopathy of prematurity grade iv rop grade iv retinopathy of prematurity grade four rop grade four retinopathy of prematurity grade one rop grade one retinopathy of prematurity pigmentary pigmentary abnormality pigmentary dispersion syndrome pigmentary glaucoma pigmentary retinopathy retinitis pigmentosa

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'pigmentary retinopathy'

Date index:2023-07-31 -

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Translation of "pigmentary retinopathy " (English → French) :

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