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 contribution||McCune-Albright syndrome|
|Number of pages||3|
|Publication status||Published - 1991|
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