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dc.contributor.author | Sudhakara Reddy, R. | es |
dc.contributor.author | Ramesh, T. | es |
dc.contributor.author | Vijayalaxmi, N. | es |
dc.contributor.author | Lavanya Reddy, R. | es |
dc.contributor.author | Swapna, L.A. | es |
dc.contributor.author | Rajesh Singh, T. | es |
dc.date.accessioned | 2014-05-21T12:41:55Z | |
dc.date.available | 2014-05-21T12:41:55Z | |
dc.date.issued | 2012 | es |
dc.identifier.citation | Sudhakara Reddy, R. ; Ramesh, T. ; Vijayalaxmi, N. ; Lavanya Reddy, R. ; Swapna, L.A. ; Rajesh Singh, T.. van der Woude syndrome- a syndromic form of orofacial clefting. En: Journal of Clinical and Experimental Dentistry, 2012, Vol. 4, No. 2: 125-128 | es |
dc.identifier.uri | http://hdl.handle.net/10550/35253 | |
dc.description.abstract | 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 degree of penetrance with cardinal clinical features of lip pits with a cleft lip, cleft palate, or both. This case report describes van der Woude syndrome in a 19 year old male patient with a specifi c reference to the various aspects of this condition, as clinical appearance, etiological factors (genetic aspects), differential diagnosis, investigative procedures and management. | en_US |
dc.subject | Odontología | es |
dc.subject | Ciencias de la salud | es |
dc.title | van der Woude syndrome- a syndromic form of orofacial clefting | es |
dc.type | journal article | es_ES |
dc.subject.unesco | UNESCO::CIENCIAS MÉDICAS | es |
dc.type.hasVersion | VoR | es_ES |