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Article

Clinical and endocrine characteristics and genetic analysis of Korean children with McCune-Albright syndrome: a retrospective cohort study.

Orphanet journal of rare diseases - 9 Aug 2016

Cho Eun-Kyung, Kim Jinsup, Yang Aram, Ki Chang-Seok, Lee Ji-Eun, Cho Sung Yoon, Jin Dong-Kyu

Abstract excerpt

BACKGROUND: McCune-Albright syndrome (MAS) is a rare disease defined by the triad of fibrous dysplasia (FD), café au lait spots, and peripheral precocious puberty (PP). Because of the rarity of this disease, only a few individuals with MAS have been reported in Korea. We describe the various clinical and endocrine manifestations and genetic analysis of 14 patients with MAS in Korea. METHODS: Patients' clinical...

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Identifiers

PMID: 27506760
DOI: 10.1186/s13023-016-0496-x
PMCID: PMC4977675

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GNAS

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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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