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Article

Branch retinal artery occlusion associated with compound heterozygous genotype for methylenetetrahydrofolate reductase.

Documenta ophthalmologica. Advances in ophthalmology - 1 May 2007

Heur Martin, Kosmorsky Gregory S, Peachey Neal S, Bala Elisa

Abstract excerpt

We present a case in which mfERG and OCT helped to make a diagnosis of an old BRAO in the setting of compound heterozygous MTHFR genotype. A 44-year-old woman presented for evaluation of a 10 month history of persistently cloudy vision OS. She had been worked up previously for MS versus BRAO, and she was on coumadin, folate, and multivitamin at the time of presentation. The patient has a fraternal twin sister who...

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Source

Identifiers

PMID: 17357807
DOI: 10.1007/s10633-007-9051-3

Genes

MTHFR

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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