Central neurodegeneration in Kennedy’s disease accompanies peripheral motor dysfunction

Abstract Spinal and bulbar muscular atrophy (SBMA), or Kennedy’s disease (KD), is a rare hereditary neuromuscular disorder demonstrating commonalities with amyotrophic lateral sclerosis (ALS). The current study aimed to define functional and central nervous system abnormalities associated with SBMA...

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Detalles Bibliográficos

Principais autores:	Sicong Tu, Tiffany Li, Antonia S. Carroll, Colin J. Mahoney, William Huynh, Susanna B. Park, Robert Henderson, Steve Vucic, Matthew C. Kiernan, Cindy S-Y Lin
Formato:	Artigo
Idioma:	Inglês
Publicado:	Nature Portfolio 2024-08-01
Series:	Scientific Reports
Assuntos:	Kennedy’s disease Spinobulbar muscular atrophy Amyotrophic lateral sclerosis MRI Diffusion-weighted imaging Peripheral nerve
Acceso en liña:	https://doi.org/10.1038/s41598-024-69393-5
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