Propriospinal myoclonus: Utility of magnetic resonance diffusion tensor imaging and fiber tracking
Identifieur interne : 000323 ( France/Analysis ); précédent : 000322; suivant : 000324Propriospinal myoclonus: Utility of magnetic resonance diffusion tensor imaging and fiber tracking
Auteurs : Emmanuel Roze [France] ; Emmanuelle Apartis [France] ; Marie Vidailhet [France] ; Valérie Cochen [France] ; Yara Beaugendre [France] ; Jean-Marc Trocello [France] ; Pierre Lasjaunias [France] ; Denis Ducreux [France]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-07-30.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Diffusion Magnetic Resonance Imaging (methods), Diffusion imaging, Diffusion tensor, Humans, MRI, Male, Middle Aged, Myoclonus, Myoclonus (diagnosis), Myoclonus (physiopathology), Nerve Fibers (pathology), Nervous system diseases, Neurophysiology, Nuclear magnetic resonance imaging, Spinal Cord (pathology), Spinal Cord (physiopathology), Tracking, diffusion tensor imaging, fiber tracking, neurophysiology, propriospinal myoclonus.
- MESH :
- diagnosis : Myoclonus.
- methods : Diffusion Magnetic Resonance Imaging.
- pathology : Nerve Fibers, Spinal Cord.
- physiopathology : Myoclonus, Spinal Cord.
- Humans, Male, Middle Aged.
Abstract
Propriospinal myoclonus (PSM) is a rare movement disorder characterized by involuntary spinal‐generated muscular jerks that spread rostrally and caudally to other spinally innervated muscles. Most patients have no clear etiology, and conventional MRI of the spinal cord is generally normal. Here we report the use of magnetic resonance diffusion tensor imaging (DTI) and fiber tracking to detect tract‐specific abnormalities in a patient with propriospinal myoclonus. As the patient had the fragile‐X premutation and antithyroid antibodies, spinal cord DTI abnormalities may be related to these conditions. Tract‐specific analysis may provide new insights into the pathophysiology of propriospinal myoclonus. © 2007 Movement Disorder Society
Url:
DOI: 10.1002/mds.21562
Affiliations:
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Hospital, AP‐HP, Paris</wicri:regionArea><placeName><settlement type="city">Paris</settlement></placeName></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="sub">Official Journal of the Movement Disorder Society</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2007-07-30">2007-07-30</date><biblScope unit="vol">22</biblScope><biblScope unit="issue">10</biblScope><biblScope unit="page" from="1506">1506</biblScope><biblScope unit="page" to="1509">1509</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">EFB7C2F479C99157A30BBA90FE9B472FF8780D13</idno><idno type="DOI">10.1002/mds.21562</idno><idno type="ArticleID">MDS21562</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Diffusion Magnetic Resonance Imaging (methods)</term><term>Diffusion imaging</term><term>Diffusion tensor</term><term>Humans</term><term>MRI</term><term>Male</term><term>Middle Aged</term><term>Myoclonus</term><term>Myoclonus (diagnosis)</term><term>Myoclonus (physiopathology)</term><term>Nerve Fibers (pathology)</term><term>Nervous system diseases</term><term>Neurophysiology</term><term>Nuclear magnetic resonance imaging</term><term>Spinal Cord (pathology)</term><term>Spinal Cord (physiopathology)</term><term>Tracking</term><term>diffusion tensor imaging</term><term>fiber tracking</term><term>neurophysiology</term><term>propriospinal myoclonus</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Myoclonus</term></keywords><keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Diffusion Magnetic Resonance Imaging</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Nerve Fibers</term><term>Spinal Cord</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Myoclonus</term><term>Spinal Cord</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Humans</term><term>Male</term><term>Middle Aged</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Imagerie RMN</term><term>Imagerie de diffusion</term><term>Myoclonie</term><term>Neurophysiologie</term><term>Pistage</term><term>Système nerveux pathologie</term><term>Tenseur de diffusion</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Propriospinal myoclonus (PSM) is a rare movement disorder characterized by involuntary spinal‐generated muscular jerks that spread rostrally and caudally to other spinally innervated muscles. Most patients have no clear etiology, and conventional MRI of the spinal cord is generally normal. Here we report the use of magnetic resonance diffusion tensor imaging (DTI) and fiber tracking to detect tract‐specific abnormalities in a patient with propriospinal myoclonus. As the patient had the fragile‐X premutation and antithyroid antibodies, spinal cord DTI abnormalities may be related to these conditions. Tract‐specific analysis may provide new insights into the pathophysiology of propriospinal myoclonus. © 2007 Movement Disorder Society</div></front></TEI><affiliations><list><country><li>France</li></country><region><li>Île-de-France</li></region><settlement><li>Créteil</li><li>Paris</li></settlement></list><tree><country name="France"><noRegion><name sortKey="Roze, Emmanuel" sort="Roze, Emmanuel" uniqKey="Roze E" first="Emmanuel" last="Roze">Emmanuel Roze</name></noRegion><name sortKey="Apartis, Emmanuelle" sort="Apartis, Emmanuelle" uniqKey="Apartis E" first="Emmanuelle" last="Apartis">Emmanuelle Apartis</name><name sortKey="Apartis, Emmanuelle" sort="Apartis, Emmanuelle" uniqKey="Apartis E" first="Emmanuelle" last="Apartis">Emmanuelle Apartis</name><name sortKey="Beaugendre, Yara" sort="Beaugendre, Yara" uniqKey="Beaugendre Y" first="Yara" last="Beaugendre">Yara Beaugendre</name><name sortKey="Beaugendre, Yara" sort="Beaugendre, Yara" uniqKey="Beaugendre Y" first="Yara" last="Beaugendre">Yara Beaugendre</name><name sortKey="Cochen, Valerie" sort="Cochen, Valerie" uniqKey="Cochen V" first="Valérie" last="Cochen">Valérie Cochen</name><name sortKey="Cochen, Valerie" sort="Cochen, Valerie" uniqKey="Cochen V" first="Valérie" last="Cochen">Valérie Cochen</name><name sortKey="Ducreux, Denis" sort="Ducreux, Denis" uniqKey="Ducreux D" first="Denis" last="Ducreux">Denis Ducreux</name><name sortKey="Lasjaunias, Pierre" sort="Lasjaunias, Pierre" uniqKey="Lasjaunias P" first="Pierre" last="Lasjaunias">Pierre Lasjaunias</name><name sortKey="Roze, Emmanuel" sort="Roze, Emmanuel" uniqKey="Roze E" first="Emmanuel" last="Roze">Emmanuel Roze</name><name sortKey="Trocello, Jean Arc" sort="Trocello, Jean Arc" uniqKey="Trocello J" first="Jean-Marc" last="Trocello">Jean-Marc Trocello</name><name sortKey="Trocello, Jean Arc" sort="Trocello, Jean Arc" uniqKey="Trocello J" first="Jean-Marc" last="Trocello">Jean-Marc Trocello</name><name sortKey="Trocello, Jean Arc" sort="Trocello, Jean Arc" uniqKey="Trocello J" first="Jean-Marc" last="Trocello">Jean-Marc Trocello</name><name sortKey="Vidailhet, Marie" sort="Vidailhet, Marie" uniqKey="Vidailhet M" first="Marie" last="Vidailhet">Marie Vidailhet</name><name sortKey="Vidailhet, Marie" sort="Vidailhet, Marie" uniqKey="Vidailhet M" first="Marie" last="Vidailhet">Marie Vidailhet</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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