TY - CHAP M1 - Book, Section TI - Wagner Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - This is a rare inherited vitreoretinopathy characterized by many optical malformations (eg, ensheathed retinal vessels, retinal pigmentation, circular membranes in a liquefied vitreous, choroidal atrophy) with a progressive clinical course that ends with optic atrophy and blindness. Other features include light-sensitive tissue that lines the retina, cataracts, and glaucoma. These may cause retinal detachment. Patients with unexplained early onset cataract or retinal detachment should be carefully evaluated for vitreoretinal degeneration. Often misdiagnosed for Stickler Syndrome; however, lacks the systemic features and the high incidence of retinal detachment seen with this latter condition differs between both disorders. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164087763 ER -