Popliteal Pterygium With Van Der Woude Syndrome

Van der Woude syndrome (VWS) is an autosomal dominant syndrome due to mutation of a gene located in the long arm of chromosome 1 (1q32.3-q4) called the interferon regulatory factor-6 (IRF6) gene. VW syndrome-affected children are born with a cleft lip or palate, hypodontia (absent teeth), and bilate...

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Detalles Bibliográficos
Autores principales: Dobs, Monica, Ghamry, Mohamed A, Anvekar, Priyanka, Lohana, Petras, Ali, Syed R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8378313/
https://www.ncbi.nlm.nih.gov/pubmed/34430173
http://dx.doi.org/10.7759/cureus.16573

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8378313/
https://www.ncbi.nlm.nih.gov/pubmed/34430173
http://dx.doi.org/10.7759/cureus.16573

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