By Ulrich Schiefer, Helmut Wilhelm, William Hart, W. Hart, W.F. Hoyt
This e-book covers all proper innovations of prognosis in addition to interpretations of medical symptoms in medical Neuro-Ophthalmology. All details is very established, highlighting ‘definition’, ‘note’ and ‘pearl’, in order that it may well even be utilized by the general practitioner in the course of the sufferer stumble upon. The integrated circulate chart posters remind the healthcare professional of an important details. additional, the accompanying lively CD includes: all the textual content passages in a searchable structure, interactive case demonstrations, lively sequences of medical indicators and video recordings of medical examinations. This designated and functional advisor deals worthy and sensible recommendation for physicians treating sufferers with neuro-ophthalmic problems.
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Additional info for Clinical Neuro-Ophthalmology [electronic resource]: A Practical Guide
C The anterior and posterior portions of the afferent visual pathway with the corresponding portions of the visual field • 26 Pearl The comparatively uncommon homonymous scotomas in the inferior quadrants are associated with damage to the superior (parietal) portions of the afferent pathway. 7 c). , the part of the visual field that is always monocular (the temporal crescent), participate in forming the so-called Meyer’s loop. 7 a). , when removing drug-resistant epileptogenic tissue, resulting in a homonymous defect in the superior quadrant of the contralateral visual field or a defect in the contralateral temporal crescent.
Using this type of strategy allows for a rather precise determination of the depths of a defect, although at the cost of multiple stimulus presentations and/or an increased density of stimulus locations. values that are just above expected threshold (based on agecorrected data). If the patient detects a stimulus presentation, no additional stimuli are used at that location, but if the stimulus is not seen, a stimulus of maximal intensity is presented at the location. One of three potential levels of response is thus detected at each site: normal, a relative deficit, or a maximum luminance defect.
The profile technique was actually done manually by examiners that were skilled in the control of stimulus values, manually moving the controlling levers in conventional perimeters then being used for kinetic testing. The advent of microprocessors was the enabling technology for further development of the static methods. The manual technique was too complex for use in patterns of more than a linear sequence, but with the automated algorithms of the microprocessor, patterns of arbitrary complexity could be exploited.
Clinical Neuro-Ophthalmology [electronic resource]: A Practical Guide by Ulrich Schiefer, Helmut Wilhelm, William Hart, W. Hart, W.F. Hoyt