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Wandering eye syndrome (WES) is a rarely reported condition. There is little information on its etiology, presenting features, pattern of inheritance and long term evolution. To investigate the clinical presentation, clinical characteristics and inheritance of WES in a cohort of Greek children. We included patients with WES with onset of symptoms before 3 years of age referred to the Department of Ophthalmology of the University of Athens, in a prospective cohort study. We performed detailed ophthalmological examination and comprehensive ocular imaging. Thirty four patients (37 eyes) were included. All the patients presented clinical features of WES in the first 3 years of life, starting with blurring of vision (85.3%). Visual acuity was severely impaired in 85.3% of the patients. All patients showed retinal thinning in the superior quadrants and in all the 30 eyes studied with optical coherence tomography, with scalloping of the edges of the foveal avascular zone and beading of the retina was evident in 27.5%. There was a very high proportion of consanguinity in our study population. Examination of parental origin revealed that most patients presented features consistent with X-linked
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