Deep brain stimulation in myoclonus–dystonia syndrome
Identifieur interne : 003270 ( Istex/Curation ); précédent : 003269; suivant : 003271Deep brain stimulation in myoclonus–dystonia syndrome
Auteurs : Laura Cif [France] ; Enza Maria Valente [Italie] ; Simone Hemm [France] ; Christine Coubes [France] ; Nathalie Vayssiere [France] ; Stéphanie Serrat [France] ; Annalisa Di Giorgio [Italie] ; Philippe Coubes [France]Source :
- Movement Disorders [ 0885-3185 ] ; 2004-06.
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Abstract
Myoclonus–dystonia syndrome (MDS) is an autosomal dominant disorder characterized by bilateral myoclonic jerks. An 8‐year‐old boy presenting with early onset, medically intractable, MDS due to a mutation in the ϵ‐sarcoglycan gene (SGCE) underwent chronic bilateral stimulation of the globus pallidus internus, which eliminates both myoclonus and dystonia. We conclude that deep brain stimulation can be an effective and safe treatment for MDS. © 2004 Movement Disorder Society
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DOI: 10.1002/mds.20030
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An 8‐year‐old boy presenting with early onset, medically intractable, MDS due to a mutation in the ϵ‐sarcoglycan gene (SGCE) underwent chronic bilateral stimulation of the globus pallidus internus, which eliminates both myoclonus and dystonia. We conclude that deep brain stimulation can be an effective and safe treatment for MDS. © 2004 Movement Disorder Society</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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