Three cases of focal dermal hypoplasia (Goltz syndrome)

M. F. Sacoor*, M. H. Motswaledi

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)

Abstract

Focal dermal hypoplasia or Goltz syndrome is a rare genodermatosis, characterized by multiple abnormalities of ectodermal and mesodermal origin. It is found predominantly in females and is characterized by hypoplasia of skin and papillomas. Three cases of focal dermal hypoplasia in infancy with unusual inheritance patterns are reported. Cutaneous features were atrophic reticulated scars involving the trunk and extremities following the lines of Blaschko. Papillomas were present on the genitalia and in a periorificial distribution. Skeletal abnormalities included syndactyly, polydactyly and lobster claw deformities. Ophthalmological examination revealed strabismus and retinal colobomas.

Original languageEnglish
Pages (from-to)35-37
Number of pages3
JournalClinical and Experimental Dermatology
Volume30
Issue number1
DOIs
Publication statusPublished - Jan 2005

Fingerprint

Dive into the research topics of 'Three cases of focal dermal hypoplasia (Goltz syndrome)'. Together they form a unique fingerprint.

Cite this