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

Jaksic, Vesna

MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion. [electronic resource] - Ophthalmic research 2010 - 193-6 p. digital

Publication Type: Case Reports; Journal Article

1423-0259

10.1159/000272023 doi


Adult
Antihypertensive Agents--therapeutic use
Glaucoma, Open-Angle--blood
Gonioscopy
Homocysteine--blood
Homozygote
Humans
Hyperhomocysteinemia--genetics
Intraocular Pressure
Male
Methylenetetrahydrofolate Reductase (NADPH2)--genetics
Mutation--genetics
Polymorphism, Single Nucleotide--genetics
Retinal Vein Occlusion--blood