Distrofia di coni e bastoncelli
Sign in to saveAlso known as retinal cone dystrophy, RCD1, Retinal Cone Degeneration, RETINAL CONE DYSTROPHY 1; RCD1, Cone Dystrophy, Autosomal Dominant, RETINAL CONE DYSTROPHY 1
inherited ocular disorder characterized by the loss of cone cells
Research
6,587 papers- Progressive Cone Dystrophy and Cone-Rod Dystrophy.Advances in experimental medicine and biology · 2025
- Progressive Cone Dystrophy and Cone-Rod Dystrophy (XL, AD, and AR).Advances in experimental medicine and biology · 2018
- Endoplasmic reticulum stress: molecular mechanism and therapeutic targets.Signal transduction and targeted therapy · 2023
- Cone dystrophy associated with autoimmune polyglandular syndrome type 1.Scientific reports · 2023
- Optical Gap Biomarker in Cone-Dominant Retinal Dystrophy.American journal of ophthalmology · 2020
via PubMed
Wikidata facts
- Subclass of
- retinal disease
- Image
- Fundus of a patient with cone rod dystrophy.png
Show 4 more facts
- health specialty
- ophthalmology
- Commons category
- Cone dystrophy
- exact match
- www.orpha.net/ORDO/Orphanet_1871
- on focus list of Wikimedia project
- WikiProject Medicine
Sources (2)
via Wikidata · CC0
Article · Italiano
La distrofia di coni e bastoncelli o sindrome di Zapfen-Stäbchen è una malattia genetica che colpisce l'occhio e comporta una progressiva diminuzione dell'acuità visiva, fino ad arrivare talvolta alla cecità completa. È considerata una variante della retinite pigmentosa, anche se la sua incidenza risulta essere molto inferiore.
Abstract from DBpedia / Wikipedia · CC BY-SA