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Page 1
Treatment of lower lip pits in Van der Woude syndrome: a systematic review.
Peralta-Mamani M, Terrero-Pérez Á, Dalben G, Rubira CMF, Honório HM, Rubira-Bullen IF. Peralta-Mamani M, et al. Int J Oral Maxillofac Surg. 2018 Apr;47(4):421-427. doi: 10.1016/j.ijom.2017.10.002. Epub 2017 Oct 28. Int J Oral Maxillofac Surg. 2018. PMID: 29089202 Review.
The presence of lower lip pits in individuals with Van der Woude syndrome (VWS) may cause discomfort due to saliva secretion. ...
The presence of lower lip pits in individuals with Van der Woude syndrome (VWS) may cause discomfort due to sali …
Clefting syndromes.
Drew SJ. Drew SJ. Atlas Oral Maxillofac Surg Clin North Am. 2014 Sep;22(2):175-81. doi: 10.1016/j.cxom.2014.05.001. Atlas Oral Maxillofac Surg Clin North Am. 2014. PMID: 25171998 Review. No abstract available.
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 …
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 …
Surgical management of lower lip pits in Van der Woude syndrome.
Bertin H, Diallo-Hornez G, Isidor B, Mercier J. Bertin H, et al. J Stomatol Oral Maxillofac Surg. 2018 Feb;119(1):67-70. doi: 10.1016/j.jormas.2017.09.003. Epub 2017 Sep 8. J Stomatol Oral Maxillofac Surg. 2018. PMID: 28893716 Review.
Van der Woude syndrome (VDWS) is characterized by the presence of lower lip pits which may be of concern to patients due to aesthetic considerations. ...
Van der Woude syndrome (VDWS) is characterized by the presence of lower lip pits which may be of concern to pati …
Syngnathia and Van der Woude syndrome: a case report and literature review.
Puvabanditsin S, Garrow E, Sitburana O, Avila FM, Nabong MY, Biswas A. Puvabanditsin S, et al. Cleft Palate Craniofac J. 2003 Jan;40(1):104-6. doi: 10.1597/1545-1569_2003_040_0104_savdws_2.0.co_2. Cleft Palate Craniofac J. 2003. PMID: 12498614 Review.
We review the literature and present a case of syngnathia associated with Van der Woude syndrome. Syngnathia can have very different etiologies, but this has rarely been reported in Van der Woude syndrome. ...Clinical implic …
We review the literature and present a case of syngnathia associated with Van der Woude syndrome. Syngnathia can …
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 …
Toward an orofacial gene regulatory network.
Kousa YA, Schutte BC. Kousa YA, et al. Dev Dyn. 2016 Mar;245(3):220-32. doi: 10.1002/dvdy.24341. Epub 2015 Sep 17. Dev Dyn. 2016. PMID: 26332872 Free PMC article. Review.
Among these, variants in interferon regulatory factor 6 (IRF6) cause syndromic orofacial clefting and contribute risk toward isolated cleft lip and palate (1/700 live births). Rare variants in IRF6 can lead to Van der Woude syndrome (1/35,000 live birt …
Among these, variants in interferon regulatory factor 6 (IRF6) cause syndromic orofacial clefting and contribute risk toward isolated cleft …
Developmental disorders of the dentition: an update.
Klein OD, Oberoi S, Huysseune A, Hovorakova M, Peterka M, Peterkova R. Klein OD, et al. Am J Med Genet C Semin Med Genet. 2013 Nov;163C(4):318-32. doi: 10.1002/ajmg.c.31382. Epub 2013 Oct 4. Am J Med Genet C Semin Med Genet. 2013. PMID: 24124058 Free PMC article. Review.
This is followed by a discussion of isolated as well as syndromic tooth agenesis, including Van der Woude syndrome (VWS), ectodermal dysplasias (EDs), oral-facial-digital (OFD) syndrome type I, Rieger syndrome, holoprosencephaly, and tooth anomalies as …
This is followed by a discussion of isolated as well as syndromic tooth agenesis, including Van der Woude syndrome …
Grainyhead-like Transcription Factors in Craniofacial Development.
Carpinelli MR, de Vries ME, Jane SM, Dworkin S. Carpinelli MR, et al. J Dent Res. 2017 Oct;96(11):1200-1209. doi: 10.1177/0022034517719264. Epub 2017 Jul 11. J Dent Res. 2017. PMID: 28697314 Review.
The antecedent member of this family, Drosophila grainyhead ( grh), is required for head skeleton development in fruit flies, loss or mutation of Grhl family members in mouse and zebrafish models leads to defects of both maxilla and mandible, and recently, mutations in human GRHL …
The antecedent member of this family, Drosophila grainyhead ( grh), is required for head skeleton development in fruit flies, loss or mutati …
26 results