Progressive External Ophthalmoplegia and Lattice Corneal-Dystrophy

dc.contributor.authorPetroutsos, G.en
dc.contributor.authorKitsos, G.en
dc.contributor.authorAsproudis, I.en
dc.contributor.authorMelissourgos, I.en
dc.contributor.authorPsilas, K.en
dc.date.accessioned2015-11-24T18:56:09Z
dc.date.available2015-11-24T18:56:09Z
dc.identifier.issn0181-5512-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/18993
dc.rightsDefault Licence-
dc.subjectautosomal dominanten
dc.subjectlattice corneal dystrophyen
dc.subjectprogressive external ophthalmoplegiaen
dc.titleProgressive External Ophthalmoplegia and Lattice Corneal-Dystrophyen
heal.abstractThe authors conducted a study in a family pedigree comprising 33 patients (men 16, women 17). In this pedigree there coexisted patients with progressive external ophthalmoplegia and corneal lattice dystrophy. Two patients with progressive external ophthalmoplegia and ten with lattice corneal dystrophy were found. One of our patients (propositus) suffered from both diseases. Our study proves that, in this pedigree, progressive external ophthalmoplegia and corneal lattice dystrophy have an autosomal dominant mode of inheritance.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondary<Go to ISI>://A1992KA22100003-
heal.journalNameJournal Francais D Ophtalmologieen
heal.journalTypepeer-reviewed-
heal.languagefr-
heal.publicationDate1992-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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