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...

Source: Orphanet Journal of Rare Diseases - April 10, 2020 Category: Internal Medicine Authors: Pierre-Fran çois 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 Tags: Research Source Type: research