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Article

A comprehensive endocrine description of Kennedy's disease revealing androgen insensitivity linked to CAG repeat length.

The Journal of clinical endocrinology and metabolism - 1 Aug 2002

Dejager S, Bry-Gauillard H, Bruckert E, Eymard B, Salachas F, LeGuern E, Tardieu S, Chadarevian R, Giral P, Turpin G

Abstract excerpt

Our study aims to provide a comprehensive view of the endocrine features in Kennedy's disease (KD). Twenty-two men with KD underwent detailed endocrine investigations. Clinical signs of partial androgen resistance were present in more than 80% of the patients, with gynecomastia being the most prominent. Gynecomastia was postpubertal but appeared before muscular weakness in most cases. Thirteen patients had...

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Source

Identifiers

PMID: 12161529
DOI: 10.1210/jcem.87.8.8780

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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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A comprehensive endocrine description of Kennedy's disease revealing androgen insensitivity linked to CAG repeat length.PMID 12161529Read ↗

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Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 families.Semantic proximity Read ↗

Kennedy's disease: a clinicopathologic correlation with mutations in the androgen receptor gene.Semantic proximity Read ↗

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Molecular analysis of the androgen receptor gene in Kennedy's disease. Report of two families and review of the literature.Semantic proximity Read ↗

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