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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.
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This document is a artículoDate2012
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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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