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Focal dermal hypoplasia. Goltz syndrome. A case report.
N Y State Dent J. 2001 Jan; 67(1):30-2.NY

Abstract

Focal dermal hypoplasia (Goltz syndrome) is a rare syndrome comprising developmental anomalies of tissues and organs of mesoectodermal origin. As a result, there are abnormalities of the eyes, skin, oral structures, musculoskeletal system and central nervous system. This article describes the case of a four-year-old female with focal dermal hypoplasia (FDH) who displayed many of the oral features associated with this syndrome. Her condition was complicated by recurrent episodes of facial cellulitis in relation to skin lesions of the face. This is an unusually severe case of FDH with previously unreported association of cutaneous anomalies and facial cellulitis.

Authors+Show Affiliations

Department of Oral & Maxillofacial Surgery, Nassau County Medical Center, USA.No affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

11221530

Citation

Adornato, M C., et al. "Focal Dermal Hypoplasia. Goltz Syndrome. a Case Report." The New York State Dental Journal, vol. 67, no. 1, 2001, pp. 30-2.
Adornato MC, Perras S, Penna KJ. Focal dermal hypoplasia. Goltz syndrome. A case report. N Y State Dent J. 2001;67(1):30-2.
Adornato, M. C., Perras, S., & Penna, K. J. (2001). Focal dermal hypoplasia. Goltz syndrome. A case report. The New York State Dental Journal, 67(1), 30-2.
Adornato MC, Perras S, Penna KJ. Focal Dermal Hypoplasia. Goltz Syndrome. a Case Report. N Y State Dent J. 2001;67(1):30-2. PubMed PMID: 11221530.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Focal dermal hypoplasia. Goltz syndrome. A case report. AU - Adornato,M C, AU - Perras,S, AU - Penna,K J, PY - 2001/2/28/pubmed PY - 2001/4/6/medline PY - 2001/2/28/entrez SP - 30 EP - 2 JF - The New York state dental journal JO - N Y State Dent J VL - 67 IS - 1 N2 - Focal dermal hypoplasia (Goltz syndrome) is a rare syndrome comprising developmental anomalies of tissues and organs of mesoectodermal origin. As a result, there are abnormalities of the eyes, skin, oral structures, musculoskeletal system and central nervous system. This article describes the case of a four-year-old female with focal dermal hypoplasia (FDH) who displayed many of the oral features associated with this syndrome. Her condition was complicated by recurrent episodes of facial cellulitis in relation to skin lesions of the face. This is an unusually severe case of FDH with previously unreported association of cutaneous anomalies and facial cellulitis. SN - 0028-7571 UR - https://www.unboundmedicine.com/medline/citation/11221530/Focal_dermal_hypoplasia__Goltz_syndrome__A_case_report_ L2 - https://www.diseaseinfosearch.org/result/2886 DB - PRIME DP - Unbound Medicine ER -