Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/37266
Full metadata record
DC FieldValueLanguage
dc.contributor.authorErdoğan, Çağdaş-
dc.contributor.authorTekin, Selma-
dc.contributor.authorÜnlütürk, Z.-
dc.contributor.authorGedik, D.K.-
dc.date.accessioned2021-02-02T09:24:49Z
dc.date.available2021-02-02T09:24:49Z
dc.date.issued2020-
dc.identifier.issn0019-1442-
dc.identifier.urihttps://hdl.handle.net/11499/37266-
dc.identifier.urihttps://doi.org/10.18071/isz.73.0060-
dc.description.abstractMyasthenia gravis (MG) and Guillain-Barre syndrome (GBS) are autoimmune disorders that may cause weakness in the extremities. The coexistence of MG and GBS in the same patient has rarely been reported previously. A 52-year-old male presenting with ptosis of the left eye that worsened with fatigue, especially toward evening, was evaluated in our outpatient department. His acetylcholine receptor antibody results were positive, supporting the diagnosis of MG. His medical history revealed a postinfectious acute onset of weakness in four extremities, difficulty in swallowing and respiratory failure, which was compatible with a myasthenic crisis; however, his nerve conduction studies and albuminocytologic dissociation at the time were compatible with GBS. With this case report, we aimed to mention this rare coincidental state, discuss possible diagnoses and review all other similar cases in the literature with their main features. © 2020 Ifjusagi Lap-es Konyvkiado Vallalat. All rights reserved.en_US
dc.language.isohuen_US
dc.publisherIfjusagi Lap-es Konyvkiado Vallalaten_US
dc.relation.ispartofIdeggyogyaszati Szemleen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAcetylcholine receptor antibodyen_US
dc.subjectGuillain-barre syndromeen_US
dc.subjectMyasthenia gravisen_US
dc.subjectcholinergic receptor antibodyen_US
dc.subjectimmunoglobulinen_US
dc.subjectpyridostigmineen_US
dc.subjectadulten_US
dc.subjectArticleen_US
dc.subjectcase reporten_US
dc.subjectclinical articleen_US
dc.subjectdifferential diagnosisen_US
dc.subjectdiplopiaen_US
dc.subjectdysphagiaen_US
dc.subjectGuillain Barre syndromeen_US
dc.subjecthumanen_US
dc.subjectlatent perioden_US
dc.subjectlimb weaknessen_US
dc.subjectmagnetic resonance angiographyen_US
dc.subjectmaleen_US
dc.subjectmiddle ageden_US
dc.subjectmuscle strengthen_US
dc.subjectmyasthenia gravisen_US
dc.subjectnerve blocken_US
dc.subjectnerve conductionen_US
dc.subjectnuclear magnetic resonance imagingen_US
dc.subjectprotein cerebrospinal fluid levelen_US
dc.subjectptosis (eyelid)en_US
dc.subjectrespiratory failureen_US
dc.subjecttendon reflexen_US
dc.titleMyasthenia gravis, guillain-barre syndrome, or both?en_US
dc.typeArticleen_US
dc.identifier.volume73en_US
dc.identifier.issue1-2en_US
dc.identifier.startpage60
dc.identifier.startpage60en_US
dc.identifier.endpage64en_US
dc.authorid0000-0002-6231-7834-
dc.authorid0000-0003-1999-0510-
dc.identifier.doi10.18071/isz.73.0060-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid32057206en_US
dc.identifier.scopus2-s2.0-85079360266en_US
dc.identifier.wosWOS:000545935800008en_US
dc.identifier.scopusqualityQ4-
dc.ownerPamukkale University-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.languageiso639-1hu-
item.grantfulltextnone-
item.openairetypeArticle-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Show simple item record



CORE Recommender

SCOPUSTM   
Citations

2
checked on Nov 16, 2024

WEB OF SCIENCETM
Citations

2
checked on Nov 21, 2024

Page view(s)

146
checked on Aug 24, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.