Persistent hyperplastic primary vitreous

A developmental ocular anomaly in which the primary vitreous body and its surrounding hyaloid vasculature failed to regress. It is usually unilateral and characterized by cataract; microphthalmos (small eyeballs), and retrolenticular fibrovascular tissue. (from Yanoff: Ophthalmology, 2nd ed.)

Also known as: PFVS, PHPV, congenital retinal detachment, ncRNA disease, non-syndromic congenital retinal non-attachment, persistent fetal vasculature syndrome, persistent foetal vasculature syndrome

13 clinical trials for this condition and its sub-types, 0 tagged with Persistent hyperplastic primary vitreous itself.