The French national protocol for Kennedy’s disease (SBMA): consensus diagnostic and management recommendations

BACKGROUND: Kennedy’s disease (KD), also known as spinal and bulbar muscular atrophy (SBMA), is a rare, adult-onset, X-linked recessive neuromuscular disease caused by CAG expansions in exon 1 of the androgen receptor gene (AR). The objective of the French national diagnostic and management protocol...

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Detalles Bibliográficos
Autores principales: Pradat, Pierre-François, Bernard, Emilien, Corcia, Philippe, Couratier, Philippe, Jublanc, Christel, Querin, Giorgia, Morélot Panzini, Capucine, Salachas, François, Vial, Christophe, Wahbi, Karim, Bede, Peter, Desnuelle, Claude
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149864/
https://www.ncbi.nlm.nih.gov/pubmed/32276665
http://dx.doi.org/10.1186/s13023-020-01366-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149864/
https://www.ncbi.nlm.nih.gov/pubmed/32276665
http://dx.doi.org/10.1186/s13023-020-01366-z

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