Publikace: Acute Ophthalmoplegia without Ataxia: A Case Report
Článekopen accesspeer-reviewedpublished version| dc.contributor.author | Ehler, Edvard | cze |
| dc.contributor.author | Formanová, Leona | cze |
| dc.contributor.author | Meleková, Alena | cze |
| dc.contributor.author | Mandysová, Petra | cze |
| dc.contributor.author | Vališ, Martin | cze |
| dc.date.accessioned | 2017-05-11T11:17:53Z | |
| dc.date.available | 2017-05-11T11:17:53Z | |
| dc.date.issued | 2016 | eng |
| dc.description.abstract | Background: Miller Fisher syndrome is a well-known disorder that belongs to a group of conditions with a high level of antibodies against ganglioside GQ1b. It is characterized by acute onset of ataxia, areflexia, and ophthalmoplegia. In cases of acute-onset ophthalmoplegia without ataxia, the diagnosis is more difficult; therefore, it is frequently delayed. Case Report: We report one such case of rapid onset of internal ophthalmoplegia, followed by external ophthalmoplegia. The diagnostic process was challenging, but eventually, a high level of antibodies against GQ1b confirmed the diagnosis. Because the clinical and electrophysiological findings were limited only to the presence of anti-GQ1b antibodies, a combination with a generalized form of Guillain-Barre syndrome could be excluded. Conclusion: Consequently, the patient was not treated with immunotherapy. At 4 months, the patient had made a good recovery. | eng |
| dc.description.abstract-translated | Pozadí: Miller Fisherův syndrom je dobře známá klinická jednotka s vysokou hladinou protilátek proti gangliozidu GQ1b. Je charakterizován ataxií, areflexií a oftalmoplegií. U případů s akutní oftalmoplegií bez ataxie bývá diagnóza vždy opožděná. Kazuistika: Prezentujeme nemocného s rychle nastupující vnitřní oftalmoplegií, později se přidala i částečná zevní oftalmoplegie. Diagnostický proces byl obtížný a nakonec až vysoká hladina anti-GQ1b protilátek vedla ke správné diagnóze. Pomocí neurofyziologické vyšetření jsme vyloučili kombinaci s generalizovanou formou Guillain-Barrého syndromu. Závěr: Nemocný s izolovanou akutní a převážně jen vnitřní oftalmoplegií nebyl léčen imunoterapií. V průběhu 4 měsíců se oftalmoplegie zcela upravila. | cze |
| dc.format | p. 1-3 | eng |
| dc.identifier.doi | 10.4172/2165-7920.1000791 | |
| dc.identifier.issn | 2165-7920 | eng |
| dc.identifier.obd | 39877935 | eng |
| dc.identifier.uri | https://hdl.handle.net/10195/67679 | |
| dc.language.iso | eng | eng |
| dc.peerreviewed | yes | eng |
| dc.publicationstatus | published version | eng |
| dc.relation.ispartof | Journal of Clinical Case Reports, volume 6, issue: 5 | eng |
| dc.relation.publisherversion | https://www.omicsgroup.org/journals/acute-ophthalmoplegia-without-ataxia-a-case-report-2165-7920-1000791.php?aid=75531 | |
| dc.rights | open access | eng |
| dc.subject | Miller Fisher syndrome | eng |
| dc.subject | Antibodies against GQ1b | eng |
| dc.subject | Ophthalmoplegia | eng |
| dc.subject | Immunotherapy | eng |
| dc.subject | Miller Fisher syndrome | cze |
| dc.subject | Protilátky proti GQ1b | cze |
| dc.subject | Oftalmoplegie | cze |
| dc.subject | Imunoterapie | cze |
| dc.title | Acute Ophthalmoplegia without Ataxia: A Case Report | eng |
| dc.title.alternative | Akutní oftalmoplegie bez ataxie: kazuistika | cze |
| dc.type | Article | eng |
| dspace.entity.type | Publication |
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