Vertical oculomotor disorders in progressive supranuclear palsy and spino-cerebellar degeneration
We performed neuro-otological investigation of vertical oculomotor disorders in 35 patients with degenerative disease [progressive supranuclear palsy (PSP) and spino-cerebellar degeneration], and obtained the following results: 1) In the patients with PSP, in addition to vertical oculogyric disorder...
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Veröffentlicht in: | Nippon Jibi Inkoka Gakkai Kaiho 1997, Vol.100 (7), p.770-781 |
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description | We performed neuro-otological investigation of vertical oculomotor disorders in 35 patients with degenerative disease [progressive supranuclear palsy (PSP) and spino-cerebellar degeneration], and obtained the following results: 1) In the patients with PSP, in addition to vertical oculogyric disorder both saccade and pursuit eye movements were disturbed, and the disturbance of saccade movement was greater. Even the patients without an oculogyric disorder were all found to have decreased saccade velocity, suggesting that this disorder may occur earliest in PSP. 2) In olivo-ponto-cerebellar atrophy (OPCA), saccade movement was less disturbed than that in PSP. In contrast, pursuit movement was disturbed more frequently. 3) In late cortical cerebellar atrophy (LCCA), vertical ocular movement was hardly disturbed compared with OPCA. 4) Concerning dentate nuclear degeneration, we cannot reach a conclusion because of the few cases studied, but a variety of oculomotor disorders were seen; both saccade and pursuit movements were disturbed, but saccade movement was less disturbed than in PSP. 5) In visual suppression tests, enhancement in the light area was frequently seen in the patients with PSP and OPCA, but none with LCCA showed such change. In addition, enhancement of the light area under visual suppression was significantly correlated with vertical oculomotor disorder. |
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Even the patients without an oculogyric disorder were all found to have decreased saccade velocity, suggesting that this disorder may occur earliest in PSP. 2) In olivo-ponto-cerebellar atrophy (OPCA), saccade movement was less disturbed than that in PSP. In contrast, pursuit movement was disturbed more frequently. 3) In late cortical cerebellar atrophy (LCCA), vertical ocular movement was hardly disturbed compared with OPCA. 4) Concerning dentate nuclear degeneration, we cannot reach a conclusion because of the few cases studied, but a variety of oculomotor disorders were seen; both saccade and pursuit movements were disturbed, but saccade movement was less disturbed than in PSP. 5) In visual suppression tests, enhancement in the light area was frequently seen in the patients with PSP and OPCA, but none with LCCA showed such change. In addition, enhancement of the light area under visual suppression was significantly correlated with vertical oculomotor disorder.</description><identifier>ISSN: 0030-6622</identifier><identifier>EISSN: 1883-0854</identifier><identifier>DOI: 10.3950/jibiinkoka.100.770</identifier><identifier>PMID: 9277099</identifier><language>eng ; jpn</language><publisher>Japan</publisher><subject>Adult ; Aged ; Electrooculography ; Female ; Humans ; Male ; Middle Aged ; Nystagmus, Pathologic - physiopathology ; Saccades ; Spinocerebellar Degenerations - physiopathology ; Supranuclear Palsy, Progressive - physiopathology</subject><ispartof>Nippon Jibi Inkoka Gakkai Kaiho, 1997, Vol.100 (7), p.770-781</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3830-dba48200ae0eaebb8aacefff6893262d3151989abeb8411ae2a9446923b12b083</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9277099$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nawata, Y</creatorcontrib><creatorcontrib>Furukawa, T</creatorcontrib><creatorcontrib>Watanabe, M</creatorcontrib><creatorcontrib>Kanoh, A</creatorcontrib><title>Vertical oculomotor disorders in progressive supranuclear palsy and spino-cerebellar degeneration</title><title>Nippon Jibi Inkoka Gakkai Kaiho</title><addtitle>Nihon Jibiinkoka Gakkai Kaiho</addtitle><description>We performed neuro-otological investigation of vertical oculomotor disorders in 35 patients with degenerative disease [progressive supranuclear palsy (PSP) and spino-cerebellar degeneration], and obtained the following results: 1) In the patients with PSP, in addition to vertical oculogyric disorder both saccade and pursuit eye movements were disturbed, and the disturbance of saccade movement was greater. Even the patients without an oculogyric disorder were all found to have decreased saccade velocity, suggesting that this disorder may occur earliest in PSP. 2) In olivo-ponto-cerebellar atrophy (OPCA), saccade movement was less disturbed than that in PSP. In contrast, pursuit movement was disturbed more frequently. 3) In late cortical cerebellar atrophy (LCCA), vertical ocular movement was hardly disturbed compared with OPCA. 4) Concerning dentate nuclear degeneration, we cannot reach a conclusion because of the few cases studied, but a variety of oculomotor disorders were seen; both saccade and pursuit movements were disturbed, but saccade movement was less disturbed than in PSP. 5) In visual suppression tests, enhancement in the light area was frequently seen in the patients with PSP and OPCA, but none with LCCA showed such change. In addition, enhancement of the light area under visual suppression was significantly correlated with vertical oculomotor disorder.</description><subject>Adult</subject><subject>Aged</subject><subject>Electrooculography</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nystagmus, Pathologic - physiopathology</subject><subject>Saccades</subject><subject>Spinocerebellar Degenerations - physiopathology</subject><subject>Supranuclear Palsy, Progressive - physiopathology</subject><issn>0030-6622</issn><issn>1883-0854</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1Lw0AQhhdRaqn9A4KQk7fU2d002T1K8QsKXtRrmE0mZW2SjbuJ4L93S4ueBmaeeXl5GLvmsJJ6DXef1ljb790eVxxgVRRwxuZcKZmCWmfnbA4gIc1zIS7ZMgRrAEBnIAXM2EyLyGs9Z_hBfrQVtomrptZ1bnQ-qW1wviYfEtsng3c7TzHgm5IwDR77qWoJfTJgG34S7OskDLZ3aUWeDLVtPNW0o548jtb1V-yiiSQtT3PB3h8f3jbP6fb16WVzv00rqWLR2mCmBAASEJIxCrGipmlypaXIRS35mmul0ZBRGedIAnWW5VpIw4UBJRfs9pgbC39NFMays6E69OnJTaEstMhkwXkExRGsvAvBU1MO3nbof0oO5UFt-a82rqCMquLTzSl9Mh3Vfy8nkfIXnS96XA</recordid><startdate>1997</startdate><enddate>1997</enddate><creator>Nawata, Y</creator><creator>Furukawa, T</creator><creator>Watanabe, M</creator><creator>Kanoh, A</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>1997</creationdate><title>Vertical oculomotor disorders in progressive supranuclear palsy and spino-cerebellar degeneration</title><author>Nawata, Y ; Furukawa, T ; Watanabe, M ; Kanoh, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3830-dba48200ae0eaebb8aacefff6893262d3151989abeb8411ae2a9446923b12b083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; jpn</language><creationdate>1997</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Electrooculography</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Nystagmus, Pathologic - physiopathology</topic><topic>Saccades</topic><topic>Spinocerebellar Degenerations - physiopathology</topic><topic>Supranuclear Palsy, Progressive - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nawata, Y</creatorcontrib><creatorcontrib>Furukawa, T</creatorcontrib><creatorcontrib>Watanabe, M</creatorcontrib><creatorcontrib>Kanoh, A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Nippon Jibi Inkoka Gakkai Kaiho</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nawata, Y</au><au>Furukawa, T</au><au>Watanabe, M</au><au>Kanoh, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vertical oculomotor disorders in progressive supranuclear palsy and spino-cerebellar degeneration</atitle><jtitle>Nippon Jibi Inkoka Gakkai Kaiho</jtitle><addtitle>Nihon Jibiinkoka Gakkai Kaiho</addtitle><date>1997</date><risdate>1997</risdate><volume>100</volume><issue>7</issue><spage>770</spage><epage>781</epage><pages>770-781</pages><issn>0030-6622</issn><eissn>1883-0854</eissn><abstract>We performed neuro-otological investigation of vertical oculomotor disorders in 35 patients with degenerative disease [progressive supranuclear palsy (PSP) and spino-cerebellar degeneration], and obtained the following results: 1) In the patients with PSP, in addition to vertical oculogyric disorder both saccade and pursuit eye movements were disturbed, and the disturbance of saccade movement was greater. Even the patients without an oculogyric disorder were all found to have decreased saccade velocity, suggesting that this disorder may occur earliest in PSP. 2) In olivo-ponto-cerebellar atrophy (OPCA), saccade movement was less disturbed than that in PSP. In contrast, pursuit movement was disturbed more frequently. 3) In late cortical cerebellar atrophy (LCCA), vertical ocular movement was hardly disturbed compared with OPCA. 4) Concerning dentate nuclear degeneration, we cannot reach a conclusion because of the few cases studied, but a variety of oculomotor disorders were seen; both saccade and pursuit movements were disturbed, but saccade movement was less disturbed than in PSP. 5) In visual suppression tests, enhancement in the light area was frequently seen in the patients with PSP and OPCA, but none with LCCA showed such change. In addition, enhancement of the light area under visual suppression was significantly correlated with vertical oculomotor disorder.</abstract><cop>Japan</cop><pmid>9277099</pmid><doi>10.3950/jibiinkoka.100.770</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Electrooculography Female Humans Male Middle Aged Nystagmus, Pathologic - physiopathology Saccades Spinocerebellar Degenerations - physiopathology Supranuclear Palsy, Progressive - physiopathology |
title | Vertical oculomotor disorders in progressive supranuclear palsy and spino-cerebellar degeneration |
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