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Case Reports
. 1986 Mar-Apr;8(2):297-300.

[Goltz syndrome]

[Article in Italian]
R Pecorari, P Banin, L De Ritis, P Cioni, M Andreoli, E Ultori, C Solaroli, E Sgarbanti
  • PMID: 3786191
Case Reports

[Goltz syndrome]

[Article in Italian]
R Pecorari et al. Pediatr Med Chir. 1986 Mar-Apr.

Abstract

Goltz syndrome or focal dermal hypoplasia is a hereditary disorder, is a rare mesodermal hypoplasia found primarily in females. It is characterized by linear hypoplasia of the skin and tumors of fat or lipomatous lesions. There are significant defects of the skeleton, dental structures, eyes, soft tissues and skin. In our work an example of new-born female with this syndrome is reported, and a review of 136 cases from the literature is presented.

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