Movement Disorders (revue)

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Propriospinal myoclonus : Utility of magnetic resonance diffusion tensor imaging and fiber tracking

Identifieur interne : 001744 ( PascalFrancis/Curation ); précédent : 001743; suivant : 001745

Propriospinal 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 :

RBID : Pascal:07-0393279

Descripteurs français

English descriptors

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.
pA  
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A03   1    @0 Mov. disord.
A05       @2 22
A06       @2 10
A08 01  1  ENG  @1 Propriospinal myoclonus : Utility of magnetic resonance diffusion tensor imaging and fiber tracking
A11 01  1    @1 ROZE (Emmanuel)
A11 02  1    @1 APARTIS (Emmanuelle)
A11 03  1    @1 VIDAILHET (Marie)
A11 04  1    @1 COCHEN (Valérie)
A11 05  1    @1 BEAUGENDRE (Yara)
A11 06  1    @1 TROCELLO (Jean-Marc)
A11 07  1    @1 LASJAUNIAS (Pierre)
A11 08  1    @1 DUCREUX (Denis)
A14 01      @1 Department of Neurology, Saint-Antoine Hospital, AP-HP @2 Paris @3 FRA @Z 1 aut. @Z 3 aut. @Z 4 aut. @Z 6 aut.
A14 02      @1 CNRS UMR 7102, Paris VI University @2 Paris @3 FRA @Z 1 aut.
A14 03      @1 Department of Neurophysiology, Saint Antoine Hospital, AP-HP @2 Paris @3 FRA @Z 2 aut. @Z 5 aut. @Z 6 aut.
A14 04      @1 INSERM U732, Paris VI University @2 Paris @3 FRA @Z 2 aut. @Z 6 aut.
A14 05      @1 INSERM U679 @2 Paris @3 FRA @Z 3 aut. @Z 4 aut.
A14 06      @1 Department of Neurophysiology, Henri Mondor Hospital, AP-HP @2 Creteil @3 FRA @Z 5 aut.
A14 07      @1 Department of Neuroradiology, Bicetre Hospital, AP-HP @2 Paris @3 FRA @Z 7 aut. @Z 8 aut.
A20       @1 1506-1509
A21       @1 2007
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000161473330250
A44       @0 0000 @1 © 2007 INIST-CNRS. All rights reserved.
A45       @0 15 ref.
A47 01  1    @0 07-0393279
A60       @1 P @3 CC
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 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.
C02 01  X    @0 002B17
C02 02  X    @0 002B24A06
C02 03  X    @0 002B17C
C03 01  X  FRE  @0 Système nerveux pathologie @5 01
C03 01  X  ENG  @0 Nervous system diseases @5 01
C03 01  X  SPA  @0 Sistema nervioso patología @5 01
C03 02  X  FRE  @0 Myoclonie @5 02
C03 02  X  ENG  @0 Myoclonus @5 02
C03 02  X  SPA  @0 Mioclonia @5 02
C03 03  X  FRE  @0 Imagerie RMN @5 09
C03 03  X  ENG  @0 Nuclear magnetic resonance imaging @5 09
C03 03  X  SPA  @0 Imaginería RMN @5 09
C03 04  X  FRE  @0 Tenseur de diffusion @5 10
C03 04  X  ENG  @0 Diffusion tensor @5 10
C03 04  X  SPA  @0 Tensor de difusión @5 10
C03 05  X  FRE  @0 Pistage @5 11
C03 05  X  ENG  @0 Tracking @5 11
C03 05  X  SPA  @0 Rastreo @5 11
C03 06  X  FRE  @0 Neurophysiologie @5 12
C03 06  X  ENG  @0 Neurophysiology @5 12
C03 06  X  SPA  @0 Neurofisiología @5 12
C03 07  X  FRE  @0 Imagerie de diffusion @4 CD @5 96
C03 07  X  ENG  @0 Diffusion imaging @4 CD @5 96
C07 01  X  FRE  @0 Mouvement involontaire @5 37
C07 01  X  ENG  @0 Involuntary movement @5 37
C07 01  X  SPA  @0 Movimiento involuntario @5 37
C07 02  X  FRE  @0 Trouble neurologique @5 38
C07 02  X  ENG  @0 Neurological disorder @5 38
C07 02  X  SPA  @0 Trastorno neurológico @5 38
N21       @1 253
N44 01      @1 OTO
N82       @1 OTO

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<term>Nuclear magnetic resonance imaging</term>
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<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.</div>
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<s1>LASJAUNIAS (Pierre)</s1>
</fA11>
<fA11 i1="08" i2="1">
<s1>DUCREUX (Denis)</s1>
</fA11>
<fA14 i1="01">
<s1>Department of Neurology, Saint-Antoine Hospital, AP-HP</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>CNRS UMR 7102, Paris VI University</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
</fA14>
<fA14 i1="03">
<s1>Department of Neurophysiology, Saint Antoine Hospital, AP-HP</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>2 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</fA14>
<fA14 i1="04">
<s1>INSERM U732, Paris VI University</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>2 aut.</sZ>
<sZ>6 aut.</sZ>
</fA14>
<fA14 i1="05">
<s1>INSERM U679</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="06">
<s1>Department of Neurophysiology, Henri Mondor Hospital, AP-HP</s1>
<s2>Creteil</s2>
<s3>FRA</s3>
<sZ>5 aut.</sZ>
</fA14>
<fA14 i1="07">
<s1>Department of Neuroradiology, Bicetre Hospital, AP-HP</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
</fA14>
<fA20>
<s1>1506-1509</s1>
</fA20>
<fA21>
<s1>2007</s1>
</fA21>
<fA23 i1="01">
<s0>ENG</s0>
</fA23>
<fA43 i1="01">
<s1>INIST</s1>
<s2>20953</s2>
<s5>354000161473330250</s5>
</fA43>
<fA44>
<s0>0000</s0>
<s1>© 2007 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45>
<s0>15 ref.</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>07-0393279</s0>
</fA47>
<fA60>
<s1>P</s1>
<s3>CC</s3>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>Movement disorders</s0>
</fA64>
<fA66 i1="01">
<s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>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.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002B17</s0>
</fC02>
<fC02 i1="02" i2="X">
<s0>002B24A06</s0>
</fC02>
<fC02 i1="03" i2="X">
<s0>002B17C</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Système nerveux pathologie</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Nervous system diseases</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Sistema nervioso patología</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Myoclonie</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Myoclonus</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Mioclonia</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Imagerie RMN</s0>
<s5>09</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Nuclear magnetic resonance imaging</s0>
<s5>09</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Imaginería RMN</s0>
<s5>09</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Tenseur de diffusion</s0>
<s5>10</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Diffusion tensor</s0>
<s5>10</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Tensor de difusión</s0>
<s5>10</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Pistage</s0>
<s5>11</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Tracking</s0>
<s5>11</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Rastreo</s0>
<s5>11</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Neurophysiologie</s0>
<s5>12</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Neurophysiology</s0>
<s5>12</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Neurofisiología</s0>
<s5>12</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Imagerie de diffusion</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Diffusion imaging</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Mouvement involontaire</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Involuntary movement</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Movimiento involuntario</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Trouble neurologique</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Neurological disorder</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Trastorno neurológico</s0>
<s5>38</s5>
</fC07>
<fN21>
<s1>253</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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