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Causes and Anatomical Site of Blindness and Severe Visual Loss in Isfahan, Islamic Republic of Iran Publisher Pubmed



Dehghan A1 ; Kianersi F1 ; Moazam E2 ; Ghanbari H1
Authors
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Authors Affiliations
  1. 1. Department of Ophthalmology, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Research and Development Centre, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Eastern Mediterranean Health Journal Published:2010


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.