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Article

Congenital aniridia variant: minimally abnormal irides with severe limbal stem cell deficiency.

Ophthalmology - 1 Jul 2011

Skeens Heather M, Brooks Brian P, Holland Edward J

Abstract excerpt

PURPOSE: To clinically and molecularly characterize a group of patients with progressive limbal stem cell deficiency (LSCD) due to aniridic keratopathy (AK), but with minimally affected irides. DESIGN: Retrospective case series. PARTICIPANTS: A total of 12 eyes of 6 patients who underwent keratolimbal allograft (KLAL) for AK in the absence of the classic stigmata of aniridia at the Cincinnati Eye...

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Source

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Identifiers

PMID: 21376398
DOI: 10.1016/j.ophtha.2010.11.021
PMCID: PMC11492833

Genes

PAX6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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