Movement Disorders (revue)

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Bilateral Striatal Necrosis, Dystonia and Multiple Mitochondrial DNA Deletions : Case Study and Effect of Deep Brain Stimulation

Identifieur interne : 002A84 ( Main/Exploration ); précédent : 002A83; suivant : 002A85

Bilateral Striatal Necrosis, Dystonia and Multiple Mitochondrial DNA Deletions : Case Study and Effect of Deep Brain Stimulation

Auteurs : Maria Stella Aniello [Italie] ; Davide Martino [Italie] ; Vittoria Petruzzella [Italie] ; Roberto Eleopra [Italie] ; Michelangelo Mancuso [Italie] ; Rosa Dell'Aglio [Italie] ; Michele Cavallo [Italie] ; Gabriele Siciliano [Italie] ; Giovanni Defazio [Italie]

Source :

RBID : Pascal:08-0115905

Descripteurs français

English descriptors

Abstract

Bilateral striatal necrosis (BSN) is relatively rare and has been related to a wide array of causes, including nuclear and mitochondrial DNA mutations. We report the clinical vignette of a patient with a 37 years-history of generalized dystonia secondary to BSN associated with multiple mitochondrial DNA deletions of undefined origin. Globus pallidus interna deep brain stimulation produced sustained benefit, with predominant improvements in disability.


Affiliations:


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Le document en format XML

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<term>Dystonie</term>
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<div type="abstract" xml:lang="en">Bilateral striatal necrosis (BSN) is relatively rare and has been related to a wide array of causes, including nuclear and mitochondrial DNA mutations. We report the clinical vignette of a patient with a 37 years-history of generalized dystonia secondary to BSN associated with multiple mitochondrial DNA deletions of undefined origin. Globus pallidus interna deep brain stimulation produced sustained benefit, with predominant improvements in disability.</div>
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