Focal facial dermal dysplasia: bitemporal lesions resembling aplasia cutis congenita.

Abstract

Focal facial dermal dysplasia is the preferred designation for an inherited disorder characterized by congenital scarlike lesions on the temples. Review of the literature reveals a spectrum of associated facial anomalies that cannot be clearly divided into discrete clinical syndromes. To reconcile the apparent genetic diversity of previously reported cases, we postulate autosomal dominant inheritance with incomplete penetrance. An isolated case of a 4 1/2-month-old infant with typical bitemporal markings and otherwise normal facies is described.

• Authors: M L Magid, J S Prendiville, N B Esterly
• Journal: Journal of the American Academy of Dermatology (J Am Acad Dermatol) Vol. 18 Issue 5 Pt 2 Pg. 1203-7 (May 1988) ISSN: 0190-9622 [Print] United States
• PMID: 3372784 (Publication Type: Case Reports, Journal Article)

Topics

• Apgar Score
• Biopsy
• Diagnosis, Differential
• Ectodermal Dysplasia (diagnosis)
• Focal Dermal Hypoplasia (diagnosis, pathology)
• Humans
• Infant
• Male
• Skin (pathology)
• Tomography, X-Ray Computed