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Article

Novel DCN Mutation in Armenian Family With Congenital Stromal Corneal Dystrophy.

Cornea - 1 Apr 2023

Williams Dominic, Chung Doug D, Hovakimyan Anna, Davtyan Araks, Glasgow Ben J, Aldave Anthony J

Abstract excerpt

PURPOSE: Congenital stromal corneal dystrophy (CSCD) is a rare congenital, dominantly inherited disorder characterized by diffuse stromal opacification associated with mutations in the decorin gene ( DCN ). As only 5 families with genetically confirmed CSCD have been reported, the identification of a novel pedigree provides the opportunity to better characterize the phenotype and genetic basis. METHODS: An...

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Identifiers

PMID: 36534610
DOI: 10.1097/ICO.0000000000003167

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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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