X-linked retinitis pigmentosa (XLRP) is a severe form of retinitis pigmentosa (RP), a rare,
inherited retinal degenerative disorder, that causes blindness. The aim of this literature …

Background Retinitis pigmentosa (RP) are a group of incurable and inherited eye
conditions, and the leading cause of inherited blindness in people under the age of 60. The …

Background Retinitis pigmentosa is a group of genetic progressive retinal dystrophies that
may adversely affect daily life. Those with RP should develop adaptive coping strategies to …

Purpose. To assess the psychological status of keratoconus sufferers and to determine the
relationship between depression and visual impairment in this group of patients. Methods …

Objective We sought to construct and validate a patient-reported outcome measure for
screening and monitoring vision-related anxiety in patients with inherited retinal …

Purpose To assess the psychological impact and the potential relationship between
depression and visual impairment in patients with retinitis pigmentosa (RP). Methods Our …

Purpose There have been few systematic reports of vision-related activity limitations of
people with retinitis pigmentosa (RP). We report a merging of data from the National Eye …

ABSTRACT Background Type 1 Usher syndrome (USH1) is a rare disease and major cause
of genetic deaf-blindness. Deafness is present from birth while retinitis pigmentosa (RP) …

Purpose: To examine whether a noncomputerized multitasking compensatory saccadic
training program (MCSTP) for patients with hemianopia, based on a reading regimen and …

Purpose: Retinitis pigmentosa (RP) is a chronic progressive disease with no curative
treatments. Understanding the variables involved with improving patients' quality of life is …