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Article

A recurrent arcuate retinopathy in familial cone-rod dystrophy secondary to heterozygous CRX deletion.

Ophthalmic genetics - 1 Dec 2019

Khan Arif O, Neri Piergiorgio, Al Teneiji Amal Mohamed

Abstract excerpt

Purpose: To describe an arcuate retinopathy appearance in a familial cone-rod dystrophy and the underlying genetic cause.Methods: Retrospective case series of an affected three-generation family (eight affected members, eight unaffected members)Results: The proband, a 47-year-old male, noted significant visual loss since his early thirties. In addition to central macular atrophic changes, retinal examination was...

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Source

Identifiers

PMID: 31743059
DOI: 10.1080/13816810.2019.1688841

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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