Progressive external ophthalmoplegia (PEO): Presentation of a mitochondrial myopathy accompanied by electron microscope

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dc.contributor.authorAktas A.
dc.contributor.authorTasdemir M.S.
dc.contributor.authorTasdemir N.
dc.contributor.authorNergiz Y.
dc.date.accessioned2024-04-24T18:44:13Z
dc.date.available2024-04-24T18:44:13Z
dc.date.issued2010
dc.departmentDicle Üniversitesien_US
dc.description.abstractKearns-Sayre syndrome is a mitochondrial disease, presenting findings before the age of 20 and characterized by chronic progressive external ophthalmoplegia and pigmentary retinal degeneration. It affects many organs, resulting in a very wide spectrum of complications. In this work, a 24-year-old female, whose complaints first started at the age of 12, showing progressing external ophthalmoplegia and diagnosed with Kearns-Sayre disease following mitochondrial changes in muscle electron microscope investigation was presented. Ways of diagnosing in mitochondrial diseases, especially those in children were tried to be evaluated.en_US
dc.identifier.endpage157en_US
dc.identifier.issn1309-100X
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-80051586463
dc.identifier.scopusqualityQ3
dc.identifier.startpage154en_US
dc.identifier.urihttps://hdl.handle.net/11468/24611
dc.identifier.volume3en_US
dc.indekslendigikaynakScopus
dc.language.isoenen_US
dc.relation.ispartofJournal of International Dental and Medical Research
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectElectron Microscopeen_US
dc.subjectKearns-Sayre Syndromeen_US
dc.subjectMitochondrial Diseasesen_US
dc.subjectProgressive External Ophthalmoplegiaen_US
dc.titleProgressive external ophthalmoplegia (PEO): Presentation of a mitochondrial myopathy accompanied by electron microscopeen_US
dc.titleProgressive external ophthalmoplegia (PEO): Presentation of a mitochondrial myopathy accompanied by electron microscope
dc.typeArticleen_US

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