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van der Woude syndrome- a syndromic form of orofacial clefting
Repositori DSpace/Manakin
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- Investigació
- Revistes
- Journal of Clinical and Experimental Dentistry
- Journal of Clinical and Experimental Dentistry. 2012. Vol. 4, no. 2
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van der Woude syndrome- a syndromic form of orofacial clefting
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| Sudhakara Reddy, R.; Ramesh, T.; Vijayalaxmi, N.; Lavanya Reddy, R.; Swapna, L.A.; Rajesh Singh, T. | |||
| Aquest document és un/a article, creat/da en: 2012 | |||
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| 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. | |||
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