Ipoplasia dermica focale (sindrome di Goltz): Descrizione di un caso

Translated title of the contribution: Focal dermal hypoplasia (Goltz'syndrome): Report of a case

N. Russo, G. Argenziano, M. Scalvenzi, M. Delfino

Research output: Contribution to journalArticle

Abstract

The Authors report a case of a 4 years old female with a paucisymptomatic focal dermal hypoplasia. The patient presented, since her birth, growth retardation, linear and reticular, white coloured, atrophic lesions, localized on the trunk and limbs in association to areas of scarring alopecia of the scalp. The hystologic examination of an atrophic lesion demonstred a dermal hypoplasia, which included a low quote of adipose tissue. The laboratory findings, the neuropsychiatric, ophthalmologic, odontostomatologic and long bones radiologic evaluations did not show pathological signs.

Translated title of the contributionFocal dermal hypoplasia (Goltz'syndrome): Report of a case
Original languageItalian
JournalDermatologia Clinica
Volume18
Issue number1
Publication statusPublished - 1998

ASJC Scopus subject areas

  • Dermatology

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  • Cite this

    Russo, N., Argenziano, G., Scalvenzi, M., & Delfino, M. (1998). Ipoplasia dermica focale (sindrome di Goltz): Descrizione di un caso. Dermatologia Clinica, 18(1).