Title of article
Causes and anatomical site of blindness and severe visual loss in Isfahan, Islamic Republic of Iran
Author/Authors
Dehghan, A. isfahan university of medical sciences - Department of Ophthalmology, ايران , Kianersi, F. isfahan university of medical sciences - Department of Ophthalmology, ايران , Moazam, E. isfahan university of medical sciences - Research and Development Centre, ايران , Ghanbari, H. isfahan university of medical sciences - Department of Ophthalmology, ايران
From page
228
To page
232
Abstract
This study in 2005 evaluated the causes and major anatomical site of blindness and severe visual loss at a school for blind children in Isfahan province, Islamic Republic of Iran. All 211 students were examined according to the modified WHO/PBL eye examination record: 70.4% were blind, 24.3% had severe visual loss and 5.3% were visually impaired. The major causes of abnormality were hereditary factors (42.7%), prenatal/ neonatal (18.5%) and unknown etiology (35.5%). The main sites of abnormality were the retina (62.6%), whole globe (17.5%), lens (7.1%) and optic nerve (7.1%). A high proportion of parents were in a consanguineous marriage (49.2%). The pattern of blindness in Isfahan encompasses characteristics of both developed and developing countries.
Journal title
Eastern Mediterranean Health Journal
Journal title
Eastern Mediterranean Health Journal
Record number
2641423
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