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Page 1
Van der Woude Syndrome.
Scheiba N, Hartschuh W. Scheiba N, et al. Dtsch Arztebl Int. 2020 Oct 30;117(44):751. doi: 10.3238/arztebl.2020.0751. Dtsch Arztebl Int. 2020. PMID: 33439825 Free PMC article. No abstract available.
Craniofacial characteristics in Van der Woude syndrome.
Estévez-Arroyo B, Gómez-Mendo I, Romero-Maroto M, Solano-Reina E, Iglesias-Linares A. Estévez-Arroyo B, et al. Oral Dis. 2023 May;29(4):1680-1691. doi: 10.1111/odi.14187. Epub 2022 Mar 22. Oral Dis. 2023. PMID: 35286743 Free article.
AIM: To describe the particular craniofacial characteristics of Van der Woude syndrome(VWS) patients compared to patients with a non-syndromic cleft (CG1) and to a malocclusive healthy population (CG2). ...
AIM: To describe the particular craniofacial characteristics of Van der Woude syndrome(VWS) patients compared to …
Mutations in Van Der Woude Families From Ethiopia.
Eshete M, Alade A, Abate F, Mossey PA, Awotoye WA, Busch T, Hailu A, Demissie Y, Butali A. Eshete M, et al. J Craniofac Surg. 2022 Mar-Apr 01;33(2):e138-e140. doi: 10.1097/SCS.0000000000008142. J Craniofac Surg. 2022. PMID: 34643600 Free PMC article.
BACKGROUND: Van der Woude syndrome (VWS) is the most common syndromic orofacial cleft which accounts for approximately 2% of all cleft lip (CL) and/or palate cases. ...
BACKGROUND: Van der Woude syndrome (VWS) is the most common syndromic orofacial cleft which accounts for approxi …
Non-random distribution of deleterious mutations in the DNA and protein-binding domains of IRF6 are associated with Van Der Woude syndrome.
Alade AA, Buxo-Martinez CJ, Mossey PA, Gowans LJJ, Eshete MA, Adeyemo WL, Naicker T, Awotoye WA, Adeleke C, Busch T, Toraño AM, Bello CA, Soto M, Soto M, Ledesma R, Marquez M, Cordero JF, Lopez-Del Valle LM, Salcedo MI, Debs N, Li M, Petrin A, Olotu J, Aldous C, Olutayo J, Ogunlewe MO, Abate F, Hailu T, Muhammed I, Gravem P, Deribew M, Gesses M, Hassan M, Pape J, Adeniyan OA, Obiri-Yeboah S, Arthur FKN, Oti AA, Olatosi O, Miller SE, Donkor P, Dunnwald MM, Marazita ML, Adeyemo AA, Murray JC, Butali A. Alade AA, et al. Mol Genet Genomic Med. 2020 Aug;8(8):e1355. doi: 10.1002/mgg3.1355. Epub 2020 Jun 17. Mol Genet Genomic Med. 2020. PMID: 32558391 Free PMC article. Review.
Derangement in these well-organized fusion events results in Orofacial clefts (OFC). Van der Woude syndrome (VWS) is one of the most common causes of syndromic cleft lip and/or palate accounting for 2% of all cases. ...The current study was designed to …
Derangement in these well-organized fusion events results in Orofacial clefts (OFC). Van der Woude syndrome (VWS …
Rare and Multiple Hypodontia in Van der Woude Syndrome: Case Report.
Trevizan ACDS, Gonçales AGB, Centurion Pagin BS, Pagin O, Neves LTD. Trevizan ACDS, et al. Cleft Palate Craniofac J. 2023 Feb;60(2):243-248. doi: 10.1177/10556656211058265. Epub 2021 Nov 17. Cleft Palate Craniofac J. 2023. PMID: 34787023
Van der Woude syndrome (VWS) is a rare syndrome of genetic etiology, commonly occasioned by mutations in the IRF6 gene and that causes disorders in craniofacial development. ...Although some dental phenotypes have been reported in this syndrome, multip …
Van der Woude syndrome (VWS) is a rare syndrome of genetic etiology, commonly occasioned by mutations in the IRF …
Van der Woude syndrome: a review. Cardinal signs, epidemiology, associated features, differential diagnosis, expressivity, genetic counselling and treatment.
Rizos M, Spyropoulos MN. Rizos M, et al. Eur J Orthod. 2004 Feb;26(1):17-24. doi: 10.1093/ejo/26.1.17. Eur J Orthod. 2004. PMID: 14994878 Review.
Congenital pits of the lower lip constitute a rare developmental malformation, transmitted by an autosomal dominant mode, with considerable heterogeneity as regards the expression of the disorder. They are present in van der Woude syndrome (VWS), in wh …
Congenital pits of the lower lip constitute a rare developmental malformation, transmitted by an autosomal dominant mode, with considerable …
Van der Woude syndrome: dentofacial features and implications for clinical practice.
Lam AK, David DJ, Townsend GC, Anderson PJ. Lam AK, et al. Aust Dent J. 2010 Mar;55(1):51-8. doi: 10.1111/j.1834-7819.2009.01178.x. Aust Dent J. 2010. PMID: 20415912 Free article.
BACKGROUND: Van der Woude syndrome (VWS) is the most common clefting syndrome in humans. ...
BACKGROUND: Van der Woude syndrome (VWS) is the most common clefting syndrome in humans. ...
A Novel IRF6 Frameshift Mutation in a Large Chinese Pedigree With Van der Woude syndrome.
Peng Q, Qin W, Li S, Huang M, Rao C, Lu X. Peng Q, et al. Cleft Palate Craniofac J. 2022 Apr;59(4):548-553. doi: 10.1177/10556656211010909. Epub 2021 Apr 28. Cleft Palate Craniofac J. 2022. PMID: 33906476
AIMS: Van der Woude syndrome (VWS) is one of the most common craniofacial anomalies, causing significant functional and psychological burden to the patients. ...
AIMS: Van der Woude syndrome (VWS) is one of the most common craniofacial anomalies, causing significant functio …
Cognitive dysfunction in adults with Van der Woude syndrome.
Nopoulos P, Richman L, Andreasen N, Murray JC, Schutte B. Nopoulos P, et al. Genet Med. 2007 Apr;9(4):213-8. doi: 10.1097/gim.0b013e3180335abd. Genet Med. 2007. PMID: 17438385 Free article.
There is phenotypic and genotypic overlap between Van der Woude syndrome and isolated cleft of the lip and/or palate. ...METHODS: Fourteen adults with Van der Woude syndrome were compared with age- and gender-matched control …
There is phenotypic and genotypic overlap between Van der Woude syndrome and isolated cleft of the lip and/or pa …
Clinical, histomorphological and therapeutic features of the Van der Woude Syndrome: literature review and presentation of an unusual case.
Angiero F, Farronato D, Ferrante F, Paglia M, Crippa R, Rufino L, Trevisiol A, Mazzola RF, Blasi S. Angiero F, et al. Eur J Paediatr Dent. 2018 Mar;19(1):70-73. doi: 10.23804/ejpd.2018.19.01.13. Eur J Paediatr Dent. 2018. PMID: 29569458 Review.
BACKGROUND: Van der Woude syndrome (VWS), an autosomal dominant condition associated with lower lip pits and/or cleft palate, is caused by mutations in the interferon regulatory factor 6 gene (lRF6 gene). ...
BACKGROUND: Van der Woude syndrome (VWS), an autosomal dominant condition associated with lower lip pits and/or …
60 results