Congenital hereditary endothelial dystrophy type 1 (Q63269): Difference between revisions
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Distrofia endotelial hereditária congênita I (CHED I) é um raro subtipo de distrofia corneana posterior caracterizada por uma aparência difusa de vidro fosco das córneas e espessamento corneano importante desde o nascimento ou infância, sem nistagmo, com turvação visual. | |||
| description / en | description / en | ||
Congenital hereditary endothelial dystrophy I (CHED I) is a rare subtype of posterior corneal dystrophy characterised by a diffuse ground-glass appearance of the corneas and marked corneal thickening from birth or infancy without nystagmus, with blurred vision. | |||
Revision as of 10:45, 14 August 2026
Congenital hereditary endothelial dystrophy I (CHED I) is a rare subtype of posterior corneal dystrophy characterised by a diffuse ground-glass appearance of the corneas and marked corneal thickening from birth or infancy without nystagmus, with blurred vision.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1580987262 |
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| English | Congenital hereditary endothelial dystrophy type 1 |
Congenital hereditary endothelial dystrophy I (CHED I) is a rare subtype of posterior corneal dystrophy characterised by a diffuse ground-glass appearance of the corneas and marked corneal thickening from birth or infancy without nystagmus, with blurred vision. |
