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

Heur, Martin

Branch retinal artery occlusion associated with compound heterozygous genotype for methylenetetrahydrofolate reductase. [electronic resource] - Documenta ophthalmologica. Advances in ophthalmology May 2007 - 163-8 p. digital

Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.

0012-4486

10.1007/s10633-007-9051-3 doi


Adult
Electroretinography
Female
Genotype
Homocysteine--blood
Humans
Hyperhomocysteinemia--genetics
Methylenetetrahydrofolate Reductase (NADPH2)--genetics
Polymorphism, Genetic
Retinal Artery Occlusion--diagnosis
Tomography, Optical Coherence
Visual Field Tests
Visual Fields