The French national protocol for Kennedy’s disease (SBMA): consensus diagnostic and management recommendations | Orphanet Journal of Rare Diseases | Full Text

The French national protocol for Kennedy’s disease (SBMA): consensus diagnostic and management recommendations | Orphanet Journal of Rare Diseases | Full Text

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

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 gen...

Authors:Pierre-François Pradat, Emilien Bernard, Philippe Corcia, Philippe Couratier, Christel Jublanc, Giorgia Querin, Capucine Morélot Panzini, François Salachas, Christophe Vial, Karim Wahbi, Peter Bede and Claude Desnuelle

Citation:Orphanet Journal of Rare Diseases 2020 15:90

Content type:Research

Published on: 10 April 2020

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