Criswick-Schepens Syndrome (Familial Exudative Vitreoretinopathy) 858e48i ; 858e48i ; 858e48i ; 858e48i ; 858e48i ; 858e48i ; 858e48i ; 858e48i ; 858e48i ; 858e48i ; 858e48i ; 323
General: Familial exudative vitreoretinopathy, similar to retrolental fibroplasia; bilateral; slowly progressive; full-term babies; no oxygen therapy; autosomal dominant; may be inherited as X-linked or autosomal dominant condition.
Ocular: Posterior vitreous detachment of organized membranes of vitreous; snowflake-like opacities of vitreous; heterotropia of macula; subretinal exudates; retinal detachment; degenerative retinal changes; retinal hemorrhage; retinal folds; enophthalmos; phthisis; intraretinal exudate; vitreous hemorrhage; amblyopia; falciform retinal fold.
Clinical: Normal general development; normal birth weight.
Brockhurst R, et al. Uveitis. I. Gonioscopy. Am J Ophthalmol 1956; 42:545.
Criswick VG, Schepens CL. Familial exudative vitreoretinopathy. Am J Ophthalmol 1969; 68:578-594.
Ebert EM, Mukai S. Familial exudative vitreoretinopathy. Int Ophthalmol Clin 1993; 33:237-247.
Fullwood P, et al. X-linked exudative vitreoretinopathy: Clinical features and genetic linkage analysis. Br J Ophthalmol 1993; 77:168-l70.
Nicholson DH, Galvis V. Criswick-Schepens syndrome. Arch Ophthalmol 1984; 102:1519-l522.
Plager DA, et al. X-linked recessive familial exudative vitreoretinopathy. Am J Ophthalmol 1992; 114:145-l48.
Van Nouhuys CE. Signs, complications, and platelet aggregation in familial exudative vitreoretinopathy. Am J Ophthalmol 199l; 111:34-41.
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