Apert Syndrome with Glucose-6-phosphate Dehydrogenase Deficiency: A Case Report

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dc.contributor.authorTosun, G.
dc.contributor.authorSener, Y.
dc.date.accessioned2020-03-26T17:03:04Z
dc.date.available2020-03-26T17:03:04Z
dc.date.issued2006
dc.departmentSelçuk Üniversitesien_US
dc.description7th Congress of the Balkan-Stomatological-Society -- MAR 28-30, 2002 -- Kusadasi, TURKEYen_US
dc.description.abstractApert syndrome is characterized by midface hypoplasia, syndactyly of the hands and feet, proptosis of eyes, steep and flat frontal bones, and premature union of cranial sutures. Maxillary hypoplasia, deep palatal vault, anterior open bite, crowding of the dental arch, severely delayed tooth eruption, and dental malocclusion are the main oral manifestations of this syndrome. In this report, a case of Apert syndrome with glucose-6-phosphate dehydrogenase (G(6)PD) deficiency is presented. The patient, a 4-year-old male and the fourth child of healthy parents, was admitted to our department because of delayed tooth eruption. He had all the cardinal symptoms of the Apert syndrome. Clinical examination revealed that primary centrals, canines and first molars erupted; however, primary second molars and laterals had not erupted. The patient had no dental caries. Preventive treatments were applied, and subsequently, the patient was taken to long-term follow up.en_US
dc.description.sponsorshipBalkan Stomatol Socen_US
dc.identifier.citationTosun, G., Sener, Y., (2006). Apert Syndrome with Glucose-6-phosphate Dehydrogenase Deficiency: A Case Report. International Journal of Paediatric Dentistry, (16), 218-221. Doi: 10.1111/j.1365-263X.2006.00696.x
dc.identifier.doi10.1111/j.1365-263X.2006.00696.xen_US
dc.identifier.endpage221en_US
dc.identifier.issn0960-7439en_US
dc.identifier.pmid16643545en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage218en_US
dc.identifier.urihttps://dx.doi.org/10.1111/j.1365-263X.2006.00696.x
dc.identifier.urihttps://hdl.handle.net/20.500.12395/20338
dc.identifier.volume16en_US
dc.identifier.wosWOS:000239336200012en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.institutionauthorTosun, G.
dc.language.isoenen_US
dc.publisherBlackwell Publishingen_US
dc.relation.ispartofInternational Journal of Paediatric Dentistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.selcuk20240510_oaigen_US
dc.titleApert Syndrome with Glucose-6-phosphate Dehydrogenase Deficiency: A Case Reporten_US
dc.typeArticleen_US

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