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BRIDGE BRIDGE Diaspora BRIDGE
OPT 322

Ocular Neurophysiology

Allied Health Sciences
O.D Optometry
2 Unit(s) (LH 30)
Course Description
At the end of OPT 322 (Ocular Neurophysiology) course, the students should be able to: 1. desribe the parts of the brain responsible for vision; 2. identify several disorders relating lesions of the visual pathways; 3. Identify the mechanisms responsible for different kinds of visual outputs; 4. discuss neurophysiological and clinical assessments of visual function; 5. discuss neurophysiological and clinical aspect of edinger wesphal nucleus; 6. be acquainted with recent advances in the researches related to visual functions; 7. explain the effects of cortical and tectal lesions on eye movements; 8. discuss the clinical implications of visual evoked potential (VER) and electroretinogram (ERG); and 9. discuss the basic physiology, functions, and clinical correlates of the cerebral cortex (including Brodmann’s areas), limbic system, cerebellum and cranial nerves; and also, the physiological basis and importance of pupillary light reflex and accommodation-convergence reflex.
Course Outline
Detailed function of central nervous system and its relationship with ocular structures and vision. Neurophysiology of retina; physiology and functions of the supraretinal system; ganglion cell, optic nerve, lateral geniculate body, visual cortex, forebrain, superior colliculus, pre-tectal and tectal regions, cerebellum, vestibular system, inferior co1liculus. Brodmann and the 'V' classifications of the brain. Functional mappings in the brain like colour, memory and many others. Electroretinogram (ERG); electrophysiology of the visual system: Centre-Surrond configuration; transient and sustained cells, X,Y,W categories; Boycott and Dowling Schema; pre-colliculus and superior Colliculus features; Tectal Oculomotor control; Lateral geniculate physiology; striate and pre-striate cortex (in cat and monkey); Visual input to parietal and temporal lobes; the limbic system and prefrontal cortex; effects of cortical and tectal lesions and eye movements; Clinical implications of visual evoked potential (VER) and Electroretinogram (ERG).
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