Benign concentric annular macular dystrophy (Q83338): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Distrofia macular anular concêntrica benigna (DMACB) é uma distrofia macular autossômica dominante progressiva caracterizada por hipopigmentação parafoveal seguida por um fenótipo semelhante a retinite pigmentosa (nictalopia e perda de visão periférica) com uma configuração de olho de boi.
@@ description / en / description / en @@
+Benign concentric annular macular dystrophy (BCAMD) is a progressive autosomal dominant macular dystrophy characterised by parafoveal hypopigmentation followed by a retinitis pigmentosa-like phenotype (nyctalopia and peripheral vision loss) with a bull s eye configuration.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1839503243
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+CID11:ID_1839503243
@@ Property / CURIE: CID11:ID_1839503243 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1839503243
@@ Property / Canary Token: dki-india-ID_1839503243 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
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@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank

Latest revision as of 08:42, 15 August 2026

Benign concentric annular macular dystrophy (BCAMD) is a progressive autosomal dominant macular dystrophy characterised by parafoveal hypopigmentation followed by a retinitis pigmentosa-like phenotype (nyctalopia and peripheral vision loss) with a bull s eye configuration.

Language	Label	Description	Also known as
default for all languages	ID_1839503243
English	Benign concentric annular macular dystrophy	Benign concentric annular macular dystrophy (BCAMD) is a progressive autosomal dominant macular dystrophy characterised by parafoveal hypopigmentation followed by a retinitis pigmentosa-like phenotype (nyctalopia and peripheral vision loss) with a bull s eye configuration.