Retinal Vascular Hypoplasia with Persistence of Primary Vitreous
General: Bilateral congenital retinopathy characterized by retinal vascular hypopl 444g67e asia and persistence of primary vitreous; etiology unknown.
Ocular: Buphthalmos; microphthalmia; fixed and dilated pupils; neovascularization of iris; glaucoma; cataract; white opaque fibrovascular retrolental membrane; retinal detachment; vitreous hemorrhage; retinal vascular hypopl 444g67e asia.
Clinical: None.
Ryan SJ, ed. Retina, vol. II, 2nd ed. St. Louis: Mosby, 1994.
Pollard JF. Treatment of persistent primary hypoplastic primary vitreous. J Pediatr Ophthalmol Strabismus 1985; 22:180-l83.
Pruett RC. The pleomorphism and complications of posterior hyperplastic primary vitreous. Am J Ophthalmol 1975; 80:625-629.
Sneed PJ, et al. Bilateral retinal vascular hypoplasia associated with persistence of the primary vitreous: a new Clinical entity? J Pediatr Ophthalmol Strabismus 1988; 25:77-85.
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