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Article

Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report.

Arquivos brasileiros de oftalmologia - 1 Jan 2000

Takitani Guilherme Eiichi da Silva, Azevedo Alexandre Gomes Bortoloti de, Motta Fabiana Louise, Teixeira Sérgio Henrique, Sallum Juliana Maria Ferraz, Vessani Roberto Murad

Abstract excerpt

A 89-year-old Black female with a 6-year history of advanced open-angle glaucoma was referred to the Glaucoma Service of the Ophthalmology Department - Federal University of São Paulo (UNIFESP). Best-corrected visual acuity was 20/400 in the right eye and 20/60 in the left eye. Pseudoexfoliation material was observed at the iris border, angle, and the anterior lens surface. Anterior biomicroscopy revealed...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 30208148
DOI: 10.5935/0004-2749.20180084

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report.PMID 30208148Read ↗

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Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people.Semantic proximity Read ↗

LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients.Semantic proximity Read ↗

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