![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)
A rare case of familal van der woude syndrome Vallabhaneni K, Muktineni S, Avula SS, Korikani A - Int J Pedod Rehabil
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
![Interlink of Two Syndromes - Demarquay-van der Woude and Popliteal Pterygium in One Family Group | OMICS International Interlink of Two Syndromes - Demarquay-van der Woude and Popliteal Pterygium in One Family Group | OMICS International](https://www.omicsonline.org/articles-images/interdisciplinary-medicine-dental-science-symmetrical-lower-lip-pit-4-188-g001.png)
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)