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Kennedy's disease: clinical presentation and laboratory diagnosis.

Clinical and experimental neurology - 1 Jan 1993

Faragher M W, Choi W T, MacLean H E, Warne G L, Zajac J D

Abstract excerpt

Kennedy's disease is a form of progressive spinal and bulbar muscular atrophy of adult onset. This paper describes a case of Kennedy's disease and discusses the laboratory diagnosis and the underlying genetic mechanism. Three other neurological diseases, Huntington's disease, myotonic dystrophy and fragile X syndrome, which have similar genetic defects, are also discussed.

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Identifiers

PMID: 7712629

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

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Research trail→

Click a neighbor to travelStep 1 · 11 closest

Kennedy's disease: clinical presentation and laboratory diagnosis.PMID 7712629Read ↗

Perspectives of Kennedy's disease.Semantic proximity Read ↗

Kennedy's disease: pathogenesis and clinical approaches.Semantic proximity Read ↗

Phenotypic variability in Kennedy's disease: implication of the early diagnostic features.Semantic proximity Read ↗

Genotype and clinical phenotype analysis of a Family with Kennedy disease.Semantic proximity Read ↗

Kennedy's disease: unusual molecular pathologic and clinical features.Semantic proximity Read ↗

Beyond motor neurons: expanding the clinical spectrum in Kennedy's disease.Semantic proximity Read ↗

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

Genetic Counseling for Adult-Onset Spinal and Bulbar Muscular Atrophy (Kennedy Syndrome): Multiple Cases of Prenatal Testing in a Family.Semantic proximity Read ↗

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 ↗

Discordant repeat size and phenotype in Kennedy syndrome.Semantic proximity Read ↗

Kennedy's disease phenotype with positive genetic study for Kugelberg-Welander's disease: case report.Semantic proximity Read ↗

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