Volume 66, Issue 3 pp. 287-288
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Reduced stereoacuity in Williams syndrome

Laurie S. Sadler

Corresponding Author

Laurie S. Sadler

Division of Genetics, Department of Pediatrics, Department of Pediatric Ophthalmology, State University of New York at Buffalo, Children's Hospital, Buffalo

Division of Genetics, Children's Hospital of Buffalo, 219 Bryant Street, Buffalo, NY 14222Search for more papers by this author
Scott E. Olitsky

Scott E. Olitsky

Division of Genetics, Department of Pediatrics, Department of Pediatric Ophthalmology, State University of New York at Buffalo, Children's Hospital, Buffalo

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James D. Reynolds

James D. Reynolds

Division of Genetics, Department of Pediatrics, Department of Pediatric Ophthalmology, State University of New York at Buffalo, Children's Hospital, Buffalo

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Abstract

Strabismus is a frequently recognized manifestation of Williams syndrome [Greenberg and Lewis, 1988: Ophthalmology 95:1608–1612; Kapp et al., 1995: Am J Ophthalmol 119:355–360]. We recently evaluated the ophthalmologic function of 12 patients with Williams syndrome (WS), with an emphasis on binocularity. Four of 12 patients (33%) had measurable strabismus. Of the 8 remaining patients, examination of binocular function was possible in 6, all of whom demonstrated reduced stereoacuity. We speculate that subnormal binocular vision and the poor visuospatial performance observed in patients with WS may be related to abnormal brain morphogenesis in the region of the occipitoparietal cortex. © 1996 Wiley-Liss, Inc.

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