Goldmann-Favre syndrome (Q99752): Difference between revisions

@@ description / pt-br / description / pt-br @@
+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).
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/890235941
@@ Property / Canonical URI: https://id.who.int/icd/entity/890235941 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_890235941
@@ Property / CURIE: CID11:ID_890235941 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_890235941
@@ Property / Canary Token: dki-india-ID_890235941 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

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
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).