Cone rod dystrophy (Q99750): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Distrofias de cones e bastonetes (CRD) são distrofias retinianas hereditárias que pertencem ao grupo das retinopatias pigmentares. As CRD são caracterizadas por depósitos de pigmento retiniano, visíveis ao exame de fundo de olho, predominantemente localizados na região macular. A CRD é caracterizada por envolvimento primário do cone ou, às vezes, por perda concomitante de cones e bastonetes, explicando os sintomas predominantes das CRD: acuidade visual diminuída, defeitos de visão de cores, fotoaversão e diminuição da sensibilidade no campo visual central, posteriormente seguido por perda progressiva de visão periférica e cegueira noturna.
@@ description / en / description / en @@
+Cone rod dystrophies (CRDs) are inherited retinal dystrophies that belong to the group of pigmentary retinopathies. CRDs are characterised by retinal pigment deposits, visible on fundus examination, predominantly localised to the macular region. CRD is characterised by primary cone involvement or, sometimes, by concomitant loss of both cones and rods, explaining the predominant symptoms of CRDs: decreased visual acuity, colour vision defects, photoaversion and decreased sensitivity in the central visual field, later followed by progressive loss in peripheral vision and night blindness.
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+August 2026Timestamp +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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After 0
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++2026-08-15T00:00:00Z
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+Gregorian
-Precision
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 Before
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@@ Property / Collection date: 15 August 2026 / rank @@
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Latest revision as of 16:25, 16 August 2026

Cone rod dystrophies (CRDs) are inherited retinal dystrophies that belong to the group of pigmentary retinopathies. CRDs are characterised by retinal pigment deposits, visible on fundus examination, predominantly localised to the macular region. CRD is characterised by primary cone involvement or, sometimes, by concomitant loss of both cones and rods, explaining the predominant symptoms of CRDs: decreased visual acuity, colour vision defects, photoaversion and decreased sensitivity in the central visual field, later followed by progressive loss in peripheral vision and night blindness.

Language	Label	Description	Also known as
default for all languages	ID_2109196114
English	Cone rod dystrophy	Cone rod dystrophies (CRDs) are inherited retinal dystrophies that belong to the group of pigmentary retinopathies. CRDs are characterised by retinal pigment deposits, visible on fundus examination, predominantly localised to the macular region. CRD is characterised by primary cone involvement or, sometimes, by concomitant loss of both cones and rods, explaining the predominant symptoms of CRDs: decreased visual acuity, colour vision defects, photoaversion and decreased sensitivity in the central visual field, later followed by progressive loss in peripheral vision and night blindness.