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Oligodontia in pseudoxanthoma elasticum

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dc.creator Sayin, M. Ozgur
dc.creator Ozen, Tuncer
dc.creator Esenlik, Elcin
dc.creator Karahan, Nermin
dc.creator Atilla, A. Onur
dc.date 2007-04-30T21:00:00Z
dc.date.accessioned 2020-10-06T10:48:52Z
dc.date.available 2020-10-06T10:48:52Z
dc.identifier 9272ab25-2e17-4b53-adcd-bc334d48b1ca
dc.identifier 10.1016/j.tripleo.2006.12.001
dc.identifier https://avesis.sdu.edu.tr/publication/details/9272ab25-2e17-4b53-adcd-bc334d48b1ca/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/66502
dc.description Pseudoxanthoma elasticum (PXE) is an inherited disorder that has both autosomal recessive and autosomal dominant pathways and is characterized by severe malformation of elastic and collagen fibers. Clinically, 3 main groups of systemic findings involving skin, eye, and vessels emerge in the symptoms. In this report, we present the case of a patient with PXE who has agenesis of most of the permanent teeth. No previous reports in the English literature have mentioned oligodontia in PXE. Our treatment plan consisted of extraction of the upper left deciduous canine followed by fixed orthodontic treatment. Further prosthodontic rehabilitation was planned to restore the edentulous area.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Oligodontia in pseudoxanthoma elasticum
dc.type info:eu-repo/semantics/article


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