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Article

Chromosome abnormalities and the genetics of congenital corneal opacification.

Molecular vision - 1 Jan 2011

Mataftsi A, Islam L, Kelberman D, Sowden J C, Nischal K K

Abstract excerpt

Congenital corneal opacification (CCO) encompasses a broad spectrum of disorders that have different etiologies, including genetic and environmental. Terminology used in clinical phenotyping is commonly not specific enough to describe separate entities, for example both the terms Peters anomaly and sclerocornea have been ascribed to a clinical picture of total CCO, without investigating the presence or absence of...

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Share to Chromosome Aberrations
Share to Chromosomes, Human
Share to Cornea

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Corneal Opacity

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Share to Eye Proteins

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Source

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Identifiers

PMID: 21738392
PMCID: PMC3123159

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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