Lattice corneal dystrophy (Q97329): Difference between revisions
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Forma rara de distrofia corneana. Não tem manifestações sistêmicas, ao contrário do outro tipo de distrofia, distrofia corneana Lattice tipo II. A distrofia Lattice recebe esse nome pelo acúmulo de depósitos amiloides, ou fibras proteicas anormais, em todo o estroma médio e anterior. | |||
| description / en | description / en | ||
This is a rare form of corneal dystrophy. It has no systemic manifestations, unlike the other type of the dystrophy, Lattice corneal dystrophy type II. Lattice dystrophy gets its name from an accumulation of amyloid deposits, or abnormal protein fibres, throughout the middle and anterior stroma. | |||
Revision as of 13:26, 16 August 2026
This is a rare form of corneal dystrophy. It has no systemic manifestations, unlike the other type of the dystrophy, Lattice corneal dystrophy type II. Lattice dystrophy gets its name from an accumulation of amyloid deposits, or abnormal protein fibres, throughout the middle and anterior stroma.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1247885635 |
||
| English | Lattice corneal dystrophy |
This is a rare form of corneal dystrophy. It has no systemic manifestations, unlike the other type of the dystrophy, Lattice corneal dystrophy type II. Lattice dystrophy gets its name from an accumulation of amyloid deposits, or abnormal protein fibres, throughout the middle and anterior stroma. |
