Van der Woude syndrome- a syndromic form of orofacial clefting

Van der Woude Syndrome is the most common form of syndromic orofacial clefting, accounting for 2% of all cases, and has the phenotype that most closely resembles the more common non-syndromic forms. The syndrome has an autosomal dominant hereditary pattern with variable expressivity and a high degre...

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Detalles Bibliográficos
Autores principales: Sudhakara Reddy, R., Ramesh, T., Vijayalaxmi, N., Lavanya Reddy, R., Swapna, L A., Rajesh Singh, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medicina Oral S.L. 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908796/
https://www.ncbi.nlm.nih.gov/pubmed/24558537
http://dx.doi.org/10.4317/jced.50559

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908796/
https://www.ncbi.nlm.nih.gov/pubmed/24558537
http://dx.doi.org/10.4317/jced.50559

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