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Craniofacial Disorders - Orofacial Features and Peculiarities in Dental Treatment

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Syndromes with Orofacial Clefts

Author(s): Beatriz Costa, Cleide Felício de Carvalho Carrara and Vivian de Agostino Biella Passos

Pp: 57-85 (29)

DOI: 10.2174/9781681085166117010011

* (Excluding Mailing and Handling)

Abstract

Orofacial clefts are among the commonest malformations affecting mankind; even though most cases of orofacial clefts are non-syndromic, they may also manifest concomitantly with a wide array of syndromes. These syndromes with orofacial clefts often also cause diverse tooth abnormalities; knowledge on these peculiarities is fundamental for professionals to allow proper dental care for affected individuals.

Keywords: Dental care, Ectrodactyly, Ectodermal dysplasia, and cleft-lip-palate syndrome, Holoprosencephaly, Orofacial cleft, Orofaciodigital syndromes, Rapp- Hodgkin syndrome, Pierre Robin syndrome, Richieri Costa Pereira syndrome, Tooth abnormalities, Van der Woude syndrome, 22q11 deletion syndrome.

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