RESUMO

Focal dermal hypoplasia (FDH), also known as Goltz-Gorlin syndrome, is an autosomal dominant disease affecting tissues derived from the ectoderm and mesoderm. Knowledge and early diagnosis of the craniofacial alterations commonly found in patients with FDH provide oral health care professionals with effective preventive and therapeutic tools. This article aims to review the craniofacial characteristics present in FDH and the main systemic manifestations that have implications for dental management, while presenting a new case of the syndrome with novel oral findings.

Assuntos

Anormalidades Craniofaciais/diagnóstico , Hipoplasia Dérmica Focal/diagnóstico , Anormalidades Dentárias/diagnóstico , Anodontia/diagnóstico , Pré-Escolar , Dente Canino/anormalidades , Assistência Odontológica para Doentes Crônicos , Hipoplasia do Esmalte Dentário/diagnóstico , Diagnóstico Precoce , Assimetria Facial/diagnóstico , Feminino , Seguimentos , Humanos , Incisivo/anormalidades , Freio Labial/anormalidades , Dente Molar/anormalidades , Palato Duro/anormalidades , Erupção Ectópica de Dente/diagnóstico