SINDROME DI MCCUNE-ALBRIGHT

Translated title of the contribution: McCune-Albright syndrome

S. Maccari, G. Albertini, F. Fornaciari, G. Fornaciari

Research output: Contribution to journalArticle

Abstract

We describe a case of this syndrome in a 30 year old woman who presented with the classical triad of the full blown form: multiple areas of polyostotic fibrous dysplasia, typical patches of brown hypermelanosis (cafe-au-lait stains) and endocrinological aberrations with pseudoprecocious puberty manifested by menarche at 6 years of age. The paper stresses the importance of the need to recognise the early clinical signs of this syndrome.

Original languageItalian
Pages (from-to)34-36
Number of pages3
JournalDermatologia Oggi
Volume6
Issue number1
Publication statusPublished - 1991

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Polyostotic Fibrous Dysplasia
Hyperpigmentation
Menarche
Puberty
Coloring Agents

ASJC Scopus subject areas

  • Dermatology

Cite this

Maccari, S., Albertini, G., Fornaciari, F., & Fornaciari, G. (1991). SINDROME DI MCCUNE-ALBRIGHT. Dermatologia Oggi, 6(1), 34-36.

SINDROME DI MCCUNE-ALBRIGHT. / Maccari, S.; Albertini, G.; Fornaciari, F.; Fornaciari, G.

In: Dermatologia Oggi, Vol. 6, No. 1, 1991, p. 34-36.

Research output: Contribution to journalArticle

Maccari, S, Albertini, G, Fornaciari, F & Fornaciari, G 1991, 'SINDROME DI MCCUNE-ALBRIGHT', Dermatologia Oggi, vol. 6, no. 1, pp. 34-36.
Maccari S, Albertini G, Fornaciari F, Fornaciari G. SINDROME DI MCCUNE-ALBRIGHT. Dermatologia Oggi. 1991;6(1):34-36.
Maccari, S. ; Albertini, G. ; Fornaciari, F. ; Fornaciari, G. / SINDROME DI MCCUNE-ALBRIGHT. In: Dermatologia Oggi. 1991 ; Vol. 6, No. 1. pp. 34-36.
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