Goldmann-Favre syndrome (Q99752): Difference between revisions
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A síndrome de Goldmann-Favre é uma distrofia vitreorretiniana genética caracterizada por início precoce de cegueira noturna, redução bilateral da acuidade visual e achados típicos do fundo de olho (alterações degenerativas pigmentares progressivas, edema macular, retinosquise). | |||
| description / en | description / en | ||
Goldmann-Favre syndrome is a genetic vitreoretinal dystrophy characterised by early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular oedema, retinoschisis). | |||
Revision as of 16:25, 16 August 2026
Goldmann-Favre syndrome is a genetic vitreoretinal dystrophy characterised by early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular oedema, retinoschisis).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_890235941 |
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| English | Goldmann-Favre syndrome |
Goldmann-Favre syndrome is a genetic vitreoretinal dystrophy characterised by early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular oedema, retinoschisis). |
