MovDisordV3, Main, Exploration, bibRecord, 002482

A family with a hereditary form of torsion dystonia from Northern Sweden treated with bilateral pallidal deep brain stimulation

Identifieur interne : 002482 ( Main/Exploration ); précédent : 002481; suivant : 002483

A family with a hereditary form of torsion dystonia from Northern Sweden treated with bilateral pallidal deep brain stimulation

Auteurs : Patric Blomstedt [Suède] ; Marwan I. Hariz [Suède, Royaume-Uni] ; Stephen Tisch [Australie] ; Monica Holmberg [Suède] ; Tommy A. Bergenheim [Suède] ; Lars Forsgren [Suède]

Source :

Movement Disorders [ 0885-3185 ] ; 2009-12-15.

RBID : ISTEX:6A2F8BBD3EEA8EE02D63B57F6642B38A3D623397

Descripteurs français

Pascal (Inist)
- Dystonie, Pathologie du système nerveux, Stimulation cérébrale profonde, Suède, Torsion, Traitement.
Wicri :
- geographic : Suède.

English descriptors

KwdEn :
- Adult, DBS, Deep Brain Stimulation (methods), Deep brain stimulation, Dystonia, Dystonia Musculorum Deformans (genetics), Dystonia Musculorum Deformans (therapy), Family Health, Female, Globus Pallidus (physiology), Humans, Male, Middle Aged, Molecular Chaperones (genetics), Nervous system diseases, Severity of Illness Index, Sweden, Torsion, Treatment, dystonia, pallidal stimulation.
MESH :
- chemical , genetics : Molecular Chaperones.
- geographic : Sweden.
- genetics : Dystonia Musculorum Deformans.
- methods : Deep Brain Stimulation.
- physiology : Globus Pallidus.
- therapy : Dystonia Musculorum Deformans.
- Adult, Family Health, Female, Humans, Male, Middle Aged, Severity of Illness Index.

Abstract

To evaluate pallidal DBS in a non‐DYT1 form of hereditary dystonia. We present the results of pallidal DBS in a family with non‐DYT1 dystonia where DYT5 to 17 was excluded. The dystonia is following an autosomal dominant pattern. Ten members had definite dystonia and five had dystonia with minor symptoms. Four patients received bilateral pallidal DBS. Mean age was 47 years. The patients were evaluated before surgery, and “on” stimulation after a mean of 2.5 years (range 1–3) using the Burke‐Fahn‐Marsden scale (BFM). Mean BFM score decreased by 79 % on stimulation, from 42.5 ± 24 to 9 ± 6.5 at the last evaluation. Cervical involvement improved by 89%. The 2 patients with oromandibular dystonia and blepharospasm demonstrated a reduction of 95% regarding these symptoms. The present study confirms the effectiveness of pallidal DBS in a new family with hereditary primary segmental and generalized dystonia. © 2009 Movement Disorder Society

Url:

https://api.istex.fr/document/6A2F8BBD3EEA8EE02D63B57F6642B38A3D623397/fulltext/pdf

DOI: 10.1002/mds.22842

Affiliations:

Le document en format XML

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<front><div type="abstract" xml:lang="en">To evaluate pallidal DBS in a non‐DYT1 form of hereditary dystonia. We present the results of pallidal DBS in a family with non‐DYT1 dystonia where DYT5 to 17 was excluded. The dystonia is following an autosomal dominant pattern. Ten members had definite dystonia and five had dystonia with minor symptoms. Four patients received bilateral pallidal DBS. Mean age was 47 years. The patients were evaluated before surgery, and “on” stimulation after a mean of 2.5 years (range 1–3) using the Burke‐Fahn‐Marsden scale (BFM). Mean BFM score decreased by 79 % on stimulation, from 42.5 ± 24 to 9 ± 6.5 at the last evaluation. Cervical involvement improved by 89%. The 2 patients with oromandibular dystonia and blepharospasm demonstrated a reduction of 95% regarding these symptoms. The present study confirms the effectiveness of pallidal DBS in a new family with hereditary primary segmental and generalized dystonia. © 2009 Movement Disorder Society</div>
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Movement Disorders (revue)

A family with a hereditary form of torsion dystonia from Northern Sweden treated with bilateral pallidal deep brain stimulation

A family with a hereditary form of torsion dystonia from Northern Sweden treated with bilateral pallidal deep brain stimulation

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	Movement Disorders (revue)
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