About 133 results

ALLMedicine™ Van Der Woude Syndrome Center

Research & Reviews  53 results

Craniofacial characteristics in Van der Woude syndrome.
Oral Diseases; Estévez-Arroyo B, Gómez-Mendo I et. al.

Mar 15th, 2022 - 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). Retrospective case-control study. A sample of 110...

Rare and Multiple Hypodontia in Van der Woude Syndrome: Case Report.
The Cleft Palate-craniofacial Journal : Official Publicat... Trevizan ACDS, Gonçales AGB et. al.

Nov 18th, 2021 - 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. VWS is characterized by the presence of paramedian fistulas in the lower ...

Mutations in Van Der Woude Families From Ethiopia.
The Journal of Craniofacial Surgery; Eshete M, Alade A et. al.

Oct 14th, 2021 - 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. It is characterized by the presence of lower lip pits, in addition to CL, CL with or without c...

A Novel IRF6 Frameshift Mutation in a Large Chinese Pedigree With Van der Woude syndrome.
The Cleft Palate-craniofacial Journal : Official Publicat... Peng Q, Qin W et. al.

Apr 29th, 2021 - Van der Woude syndrome (VWS) is one of the most common craniofacial anomalies, causing significant functional and psychological burden to the patients. This study aimed to identify the genetic cause of VWS in a Chinese family. Whole genome sequenc...

Clinical Findings and Outcomes of Palatal Repair in 9 Patients With Van der Woude Syndr...
Annals of Plastic Surgery; Allam KA, Haredy MM

Dec 22nd, 2020 - Van der Woude syndrome (VWS), an autosomal dominant condition associated with clefts of the lip and/or palate and lower lip pits, is caused by mutations in interferon regulatory factor 6 gene. It is reported to be the most common syndromic cleft w...

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