Focal dermal hypoplasia: a case report and literature review

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. (Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2011; 112: e11-e18)Univ São Paulo, Fac Odontol, Dept Orthodont & Pediat Dent, BR-22270550 São Paulo, BrazilUniv São Paulo, Dept Pediat Dent, BR-22270550 São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Dept Morphol, São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Dept Morphol, São Paulo, BrazilWeb of Scienc