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Article

MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion.

Ophthalmic research - 1 Jan 2010

Jaksic Vesna, Markovic Vujica, Milenkovic Svetislav, Stefanovic Ivan, Jakovic Natalija, Knezevic Miroslav

Abstract excerpt

PURPOSE: We present the rare case of a young male patient with asymmetric ocular findings: pigmentary ocular hypertension associated with nonischemic central retinal vein occlusion (CRVO) in the right eye and pigmentary glaucoma (PG) with progressive glaucomatous optic damage in the left eye. PATIENTS AND METHODS: A 31-year-old man showed nonischemic CRVO in the right eye and the clinical triad of pigment...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20068371
DOI: 10.1159/000272023

Genes

MTHFR

Variants

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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