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Article

Unusual phenotypical variations in a boy with McCune-Albright syndrome.

Hormone research in paediatrics - 1 Jan 2010

Mamkin Irene, Philibert Pascal, Anhalt Henry, Ten Svetlana, Sultan Charles

Abstract excerpt

BACKGROUND: McCune-Albright syndrome (MAS) typically comprises the constellation of polyostotic fibrous dysplasia, café-au-lait spots, and associated endocrinopathies including gonadotropin-independent precocious puberty, excessive growth hormone production and gigantism, hyperthyroidism, and hyperparathyroidism. OBJECTIVE: We report the unique case of a boy with the diagnostic criteria of MAS accompanied by...

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Source

Identifiers

PMID: 20197676
DOI: 10.1159/000284365

Genes

AMH

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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