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van der Woude syndrome- a syndromic form of orofacial clefting

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van der Woude syndrome- a syndromic form of orofacial clefting

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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

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