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Focal dermal hypoplasia: a case report and literature review.

Abstract

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.

Authors+Show Affiliations

Department of Orthodontics and Pediatric Dentistry, Faculdade de Odontologia, Universidade de São Paulo, São Paulo, Brazil. chrismurakami@gmail.comNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article
Review

Language

eng

PubMed ID

21684779

Citation

Murakami, Christiana, et al. "Focal Dermal Hypoplasia: a Case Report and Literature Review." Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics, vol. 112, no. 2, 2011, pp. e11-8.
Murakami C, de Oliveira Lira Ortega A, Guimarães AS, et al. Focal dermal hypoplasia: a case report and literature review. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2011;112(2):e11-8.
Murakami, C., de Oliveira Lira Ortega, A., Guimarães, A. S., Gonçalves-Bittar, D., Bönecker, M., & Ciamponi, A. L. (2011). Focal dermal hypoplasia: a case report and literature review. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics, 112(2), e11-8. https://doi.org/10.1016/j.tripleo.2011.03.012
Murakami C, et al. Focal Dermal Hypoplasia: a Case Report and Literature Review. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2011;112(2):e11-8. PubMed PMID: 21684779.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Focal dermal hypoplasia: a case report and literature review. AU - Murakami,Christiana, AU - de Oliveira Lira Ortega,Adriana, AU - Guimarães,Antônio Sérgio, AU - Gonçalves-Bittar,Daniela, AU - Bönecker,Marcelo, AU - Ciamponi,Ana Lídia, PY - 2010/08/23/received PY - 2011/03/07/revised PY - 2011/03/08/accepted PY - 2011/6/21/entrez PY - 2011/6/21/pubmed PY - 2011/12/13/medline SP - e11 EP - 8 JF - Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics JO - Oral Surg Oral Med Oral Pathol Oral Radiol Endod VL - 112 IS - 2 N2 - 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. SN - 1528-395X UR - https://www.unboundmedicine.com/medline/citation/21684779/Focal_dermal_hypoplasia:_a_case_report_and_literature_review_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S1079-2104(11)00160-0 DB - PRIME DP - Unbound Medicine ER -