Wiedemann–Rautenstrauch Syndrome: Case Report

Basit Öğe Kaydı
dc.contributor.authorİpek, İrem
dc.contributor.authorDerdiyok, Cansu
dc.contributor.authorÖznurhan, Fatih
dc.date.accessioned2024-10-26T17:51:24Z
dc.date.available2024-10-26T17:51:24Z
dc.date.issued2022
dc.departmentSivas Cumhuriyet Üniversitesi
dc.description.abstractNeonatal-progeroid syndrome known as Wiedemann Rautenstrauch syndrome (WRS) is an extremely rare, autosomal recessive disorder. Neonatal progeroid disease characterized by progeroid appearance growth retardation, lipodystrophy, an unusual face (triangular shape, sparse hair, small mouth, macrocephaly, pointed jaw), thin skin, hard and thick joints and dental anomalies (newborn tooth; hypodontics). A 5-year-old boy case diagnosed with hypodontics is presented. In this case, a child prosthesis was performed to facilitate the nutrition of the patient and to increase the quality of life. © This work is licensed under Creative Commons Attribution 4.0 International License
dc.identifier.doi10.7126/cumudj.1127344
dc.identifier.endpage284
dc.identifier.issn2146-2852
dc.identifier.issue3
dc.identifier.scopus2-s2.0-85139999185
dc.identifier.scopusqualityQ4
dc.identifier.startpage282
dc.identifier.trdizinid1129543
dc.identifier.urihttps://doi.org/10.7126/cumudj.1127344
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1129543
dc.identifier.urihttps://hdl.handle.net/20.500.12418/26183
dc.identifier.volume25
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.language.isoen
dc.publisherCumhuriyet University Faculty of Dentistry
dc.relation.ispartofCumhuriyet Dental Journal
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAlkaline phosphatase; Orthodontics; Osteoclasts; Risedronic acid; Tooth movement
dc.titleWiedemann–Rautenstrauch Syndrome: Case Report
dc.typeArticle

Dosyalar

Koleksiyon

Scopus İndeksli Yayınlar Koleksiyonu
TR-Dizin İndeksli Yayınlar Koleksiyonu