Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/23645
Full metadata record
DC FieldValueLanguage
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.accessioned2015-11-24T19:34:42Z-
dc.date.available2015-11-24T19:34:42Z-
dc.identifier.issn0181-5512-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/23645-
dc.rightsDefault Licence-
dc.subjectAdulten
dc.subjectCorneal Dystrophies, Hereditary/*geneticsen
dc.subjectFemaleen
dc.subjectGenetic Linkageen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectOphthalmoplegia, Chronic Progressive External/*geneticsen
dc.subjectPedigreeen
dc.titleAssociation of progressive external ophthalmoplegia and lattice corneal dystrophyen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/1298770-
heal.languagefr-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate1992-
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.journalNameJ Fr Ophtalmolen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

Files in This Item:
There are no files associated with this item.


This item is licensed under a Creative Commons License Creative Commons