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Vukicevic, Meri; Le, Anh; Baglin, James – Journal of Visual Impairment & Blindness, 2012
In the typical human visual system, the macula allows for high visual resolution. Damage to this area from diseases, such as age-related macular degeneration (AMD), causes the loss of central vision in the form of a central scotoma. Since no treatment is available to reverse AMD, providing low vision rehabilitation to compensate for the loss of…
Descriptors: Teaching Methods, Pathology, Reading Comprehension, Vision
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Haddad, Herskel M.; And Others – Journal of Learning Disabilities, 1984
In 73 children (6-13 years old) with reading difficulty, ophthalmological evaluation showed that 18 had overt refractive errors, 18 dyslexia and no ocular anomalies, and 37 impaired fusional amplitudes, 24 of whom were dyslexic. In all Ss with poor fusional amplitudes the reading mechanism could be improved with orthoptic exercises. (Author/CL)
Descriptors: Dyslexia, Eyes, Ophthalmology, Vision
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van den Broek, Ellen G. C.; Janssen, C. G. C.; van Ramshorst, T.; Deen, L. – Journal of Intellectual Disability Research, 2006
Background: The prevalence of visual impairments in people with severe and profound multiple disabilities (SPMD) is the subject of considerable debate and is difficult to assess. Methods: In a typical Dutch care organization, all clients with SPMD (n = 76) participated in the study and specific instruments adapted to these clients (requiring a…
Descriptors: Visual Impairments, Incidence, Multiple Disabilities, Visual Acuity
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Aitken, S.; Buultjens, M. – Journal of Visual Impairment and Blindness, 1991
This article reports on a study of the methods that 21 ophthalmologists used to assess the visual acuity of children with multiple impairments and the difficulties they encountered. Additional means of assessing visual function and alternative means of communicating the results are suggested. (Author/DB)
Descriptors: Children, Evaluation Methods, Multiple Disabilities, Ophthalmology
Corwin, Thomas R; Mancini, Michael – 1978
A new test designed to detect an hereditary eye disease called retinitis pigmentosa (RP) is described. This condition is revealed by pigmentation in the retina, but early diagnosis is difficult because the symptoms are subtle, and since it is genetically recessive it frequently occurs in families with no history of early blindness. In many cases…
Descriptors: Eyes, Medical Research, Ophthalmology, Physiology
Robb, Richard M. – Sight Saving Rev, 1970
Descriptors: Child Development, Eyes, Identification, Infants
Flax, Marshall E.; Luchterhand, Charlene – 1998
This fact sheet uses a question-and-answer format to provide basic information about changes in vision for older adults and what kind of services are needed particularly adults with developmental disabilities. Questions address the following topics: the importance of eye exams for adults with developmental disabilities; the need for eye exams even…
Descriptors: Aging (Individuals), Developmental Disabilities, Health Services, Ophthalmology
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Hofstetter, H. W. – Journal of Visual Impairment and Blindness, 1991
Low vision children (ages 4-19, n=137) were screened, and 77 percent were advised to have comprehensive clinical evaluations or ophthalmology services. The visual capability of the referred children was determined, low vision aids were prescribed for 56 children, and the degree of successful utilization of aids was evaluated. (JDD)
Descriptors: Assistive Devices (for Disabled), Children, Clinical Diagnosis, Equipment Utilization
Johnson, Samuel B. – Sight-Saving Review, 1974
Descriptors: Adults, Disadvantaged, Economically Disadvantaged, Exceptional Child Services