Goldmann-Favre syndrome (Q99752): Difference between revisions
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15 August 2026
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Latest 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). |
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CID11:ID_890235941
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dki-india-ID_890235941
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Concluído
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15 August 2026
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