Translated title of the contribution: McCune-Albright syndrome

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

Research output: Contribution to journalArticlepeer-review


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.

Translated title of the contributionMcCune-Albright syndrome
Original languageItalian
Pages (from-to)34-36
Number of pages3
JournalDermatologia Oggi
Issue number1
Publication statusPublished - 1991

ASJC Scopus subject areas

  • Dermatology


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