DBMCI - MDS Experts : the NEET MDS Experts - VAN-DER WOUDE SYNDROME • It is genetic condition with autosomal dominant inheritance which affects development of face. CLINICAL FEATURES • Lower lip
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Van der Woude syndrome: dentofacial features and implications for clinical practice - Lam - 2010 - Australian Dental Journal - Wiley Online Library
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Interlink of Two Syndromes - Demarquay-van der Woude and Popliteal Pterygium in One Family Group | OMICS International
![Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene | Journal of Medical Genetics Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/41/2/e15/F1.large.jpg)
Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene | Journal of Medical Genetics
![A rare case of familal van der woude syndrome Vallabhaneni K, Muktineni S, Avula SS, Korikani A - Int J Pedod Rehabil A rare case of familal van der woude syndrome Vallabhaneni K, Muktineni S, Avula SS, Korikani A - Int J Pedod Rehabil](https://www.ijpedor.org/articles/2019/4/2/images/IntJPedodRehabil_2019_4_2_76_272066_f2.jpg)