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Article

A case of McCune-Albright syndrome with associated multiple endocrinopathies.

The Korean journal of internal medicine - 1 Mar 2007

Sung Sang Hun, Yoon Hyun Dae, Shon Ho Sang, Kim Hong Tae, Choi Woo Young, Seo Chang Jin, Lee Joo Hyoung

Abstract excerpt

McCune-Albright syndrome (MAS) is a rare disorder that develops from an activating mutation in the Gs gene. It is characterized by an association with Polyostotic fibrous dysplasia, and precocious puberty, Caf-au-lait pigmentation, and other endocrinopathies that result from the hyperactivity of a variety of endocrine glands. Recently we encountered a patient with MAS with fibrous dysplasia, skin pigmentation,...

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Source

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Identifiers

PMID: 17427647
DOI: 10.3904/kjim.2007.22.1.45
PMCID: PMC2687599

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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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