Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation
Identifieur interne : 004A37 ( Main/Curation ); précédent : 004A36; suivant : 004A38Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation
Auteurs : Lucia Angelini [Italie] ; Nardo Nardocci [Italie] ; Margherita Estienne [Italie] ; Chiara Conti [Italie] ; Ivano Dones [Italie] ; Giovanni Broggi [Italie]Source :
- Movement Disorders [ 0885-3185 ] ; 2000-09.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Enfant.
English descriptors
- KwdEn :
- Adolescent, Bilateral, Case study, Child, Cognition Disorders (etiology), Critically ill, Deep brain stimulation, Diagnosis, Differential, Dysarthria (etiology), Dyskinesia, Dyskinesias (etiology), Dystonia, Dystonic Disorders (complications), Dystonic Disorders (physiopathology), Dystonic Disorders (therapy), Electric Stimulation Therapy (methods), Electrical stimulus, Electrodes, Implanted, Evolution, Globus Pallidus (surgery), Humans, Instrumentation therapy, Male, Pallidal stimulation, Pallidum, Refractory, Refractory dyskinesia, Refractory dystonia, Severity of Illness Index, Stereotaxic Techniques, Treatment Outcome, Videotape Recording.
- MESH :
- complications : Dystonic Disorders.
- etiology : Cognition Disorders, Dysarthria, Dyskinesias.
- methods : Electric Stimulation Therapy.
- physiopathology : Dystonic Disorders.
- surgery : Globus Pallidus.
- therapy : Dystonic Disorders.
- Adolescent, Diagnosis, Differential, Electrodes, Implanted, Humans, Male, Severity of Illness Index, Stereotaxic Techniques, Treatment Outcome, Videotape Recording.
Abstract
We report a 13‐year‐old boy who developed severe, refractory dystonia–dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The movements became continuous, requiring artificial respiration and continuous sedation in the intensive‐care unit. Various drugs and drug combinations failed to achieve control. The child was then treated successfully with bilateral pallidal (GPi) stimulation as shown in the videotape. Four months later and without medication, the boy regained autonomous gait and audible speech; his neurologic condition continues to improve.
Url:
DOI: 10.1002/1531-8257(200009)15:5<1010::AID-MDS1039>3.0.CO;2-5
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<front><div type="abstract" xml:lang="en">We report a 13‐year‐old boy who developed severe, refractory dystonia–dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The movements became continuous, requiring artificial respiration and continuous sedation in the intensive‐care unit. Various drugs and drug combinations failed to achieve control. The child was then treated successfully with bilateral pallidal (GPi) stimulation as shown in the videotape. Four months later and without medication, the boy regained autonomous gait and audible speech; his neurologic condition continues to improve.</div>
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<term>Dystonia</term>
<term>Electrical stimulus</term>
<term>Evolution</term>
<term>Instrumentation therapy</term>
<term>Male</term>
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<front><div type="abstract" xml:lang="en">We report a 13-year-old boy who developed severe, refractory dystonia-dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The movements became continuous, requiring artificial respiration and continuous sedation in the intensive-care unit. Various drugs and drug combinations failed to achieve control. The child was then treated successfully with bilateral pallidal (GPi) stimulation as shown in the videotape. Four months later and without medication, the boy regained autonomous gait and audible speech; his neurologic condition continues to improve.</div>
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<author><name sortKey="Estienne, Margherita" sort="Estienne, Margherita" uniqKey="Estienne M" first="Margherita" last="Estienne">Margherita Estienne</name>
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<author><name sortKey="Conti, Chiara" sort="Conti, Chiara" uniqKey="Conti C" first="Chiara" last="Conti">Chiara Conti</name>
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<front><div type="abstract" xml:lang="en">We report a 13‐year‐old boy who developed severe, refractory dystonia–dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The movements became continuous, requiring artificial respiration and continuous sedation in the intensive‐care unit. Various drugs and drug combinations failed to achieve control. The child was then treated successfully with bilateral pallidal (GPi) stimulation as shown in the videotape. Four months later and without medication, the boy regained autonomous gait and audible speech; his neurologic condition continues to improve.</div>
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<front><div type="abstract" xml:lang="en">We report a 13-year-old boy who developed severe, refractory dystonia-dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The movements became continuous, requiring artificial respiration and continuous sedation in the intensive-care unit. Various drugs and drug combinations failed to achieve control. The child was then treated successfully with bilateral pallidal (GPi) stimulation as shown in the videotape. Four months later and without medication, the boy regained autonomous gait and audible speech; his neurologic condition continues to improve.</div>
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