Movement Disorders (revue)

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Adult-onset tic disorder, motor stereotypies, and behavioural disturbance associated with antibasal ganglia antibodies

Identifieur interne : 002045 ( PascalFrancis/Corpus ); précédent : 002044; suivant : 002046

Adult-onset tic disorder, motor stereotypies, and behavioural disturbance associated with antibasal ganglia antibodies

Auteurs : Mark J. Edwards ; Russell C. Dale ; Andrew J. Church ; Eleni Trikouli ; Niall P. Quinn ; Andrew J. Lees ; Gavin Giovannoni ; Kailash P. Bhatia

Source :

RBID : Pascal:04-0581920

Descripteurs français

English descriptors

Abstract

The onset of tics in adulthood is rare and, unlike the childhood variety, there is commonly a secondary environmental cause. We present four cases (1 man, 3 women) with an adult onset tic disorder (mean age of onset, 36 years; range, 27-42 years) associated with the presence of serum antibasal ganglia antibodies (ABGA). One patient had motor tics and unusual motor stereotypies, 2 had multiple motor and vocal tics, and the remaining patient had motor tics only. Concomitant psychiatric disturbance was noted in 3 cases. In 2 cases, there was a close temporal relationship between upper respiratory tract infection and the subsequent onset of tics. Imaging was possible in three cases and was normal in two but revealed a lesion involving the right caudate and lentiform nuclei in the other. We suggest that there might be a causal relationship between ABGA and the clinical syndrome in these cases and that ABGA should be considered as a possible etiology for adult-onset tics.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0885-3185
A03   1    @0 Mov. disord.
A05       @2 19
A06       @2 10
A08 01  1  ENG  @1 Adult-onset tic disorder, motor stereotypies, and behavioural disturbance associated with antibasal ganglia antibodies
A11 01  1    @1 EDWARDS (Mark J.)
A11 02  1    @1 DALE (Russell C.)
A11 03  1    @1 CHURCH (Andrew J.)
A11 04  1    @1 TRIKOULI (Eleni)
A11 05  1    @1 QUINN (Niall P.)
A11 06  1    @1 LEES (Andrew J.)
A11 07  1    @1 GIOVANNONI (Gavin)
A11 08  1    @1 BHATIA (Kailash P.)
A14 01      @1 Sobell Department of Movement Neuroscience and Movement Disorders, Institute of Neurology, University College London, Queen Square @2 London @3 GBR @Z 1 aut. @Z 4 aut. @Z 5 aut. @Z 8 aut.
A14 02      @1 Neuroimmunology unit, Department of Neuroinflammation. Institute of Neurology, University College London, Queen Square @2 London @3 GBR @Z 2 aut. @Z 3 aut. @Z 7 aut.
A14 03      @1 Neurosciences unit, Institute of Child Health. @2 London @3 GBR @Z 2 aut.
A14 04      @1 The Reta Lila Weston Institute of Neurological Studies, The Windeyer Building @2 London @3 GBR @Z 6 aut.
A20       @1 1190-1196
A21       @1 2004
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000122474340090
A44       @0 0000 @1 © 2004 INIST-CNRS. All rights reserved.
A45       @0 33 ref.
A47 01  1    @0 04-0581920
A60       @1 P @3 CC
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 The onset of tics in adulthood is rare and, unlike the childhood variety, there is commonly a secondary environmental cause. We present four cases (1 man, 3 women) with an adult onset tic disorder (mean age of onset, 36 years; range, 27-42 years) associated with the presence of serum antibasal ganglia antibodies (ABGA). One patient had motor tics and unusual motor stereotypies, 2 had multiple motor and vocal tics, and the remaining patient had motor tics only. Concomitant psychiatric disturbance was noted in 3 cases. In 2 cases, there was a close temporal relationship between upper respiratory tract infection and the subsequent onset of tics. Imaging was possible in three cases and was normal in two but revealed a lesion involving the right caudate and lentiform nuclei in the other. We suggest that there might be a causal relationship between ABGA and the clinical syndrome in these cases and that ABGA should be considered as a possible etiology for adult-onset tics.
C02 01  X    @0 002B17
C02 02  X    @0 002B17G
C02 03  X    @0 002B17F
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 Stéréotypie @5 02
C03 02  X  ENG  @0 Stereotypy @5 02
C03 02  X  SPA  @0 Estereotipia @5 02
C03 03  X  FRE  @0 Tic @5 04
C03 03  X  ENG  @0 Tic @5 04
C03 03  X  SPA  @0 Tic @5 04
C03 04  X  FRE  @0 Trouble moteur @5 07
C03 04  X  ENG  @0 Motor system disorder @5 07
C03 04  X  SPA  @0 Trastorno motor @5 07
C03 05  X  FRE  @0 Contrôle moteur @5 25
C03 05  X  ENG  @0 Motor control @5 25
C03 05  X  SPA  @0 Control motor @5 25
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       @1 334
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 04-0581920 INIST
ET : Adult-onset tic disorder, motor stereotypies, and behavioural disturbance associated with antibasal ganglia antibodies
AU : EDWARDS (Mark J.); DALE (Russell C.); CHURCH (Andrew J.); TRIKOULI (Eleni); QUINN (Niall P.); LEES (Andrew J.); GIOVANNONI (Gavin); BHATIA (Kailash P.)
AF : Sobell Department of Movement Neuroscience and Movement Disorders, Institute of Neurology, University College London, Queen Square/London/Royaume-Uni (1 aut., 4 aut., 5 aut., 8 aut.); Neuroimmunology unit, Department of Neuroinflammation. Institute of Neurology, University College London, Queen Square/London/Royaume-Uni (2 aut., 3 aut., 7 aut.); Neurosciences unit, Institute of Child Health./London/Royaume-Uni (2 aut.); The Reta Lila Weston Institute of Neurological Studies, The Windeyer Building/London/Royaume-Uni (6 aut.)
DT : Publication en série; Courte communication, note brève; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2004; Vol. 19; No. 10; Pp. 1190-1196; Bibl. 33 ref.
LA : Anglais
EA : The onset of tics in adulthood is rare and, unlike the childhood variety, there is commonly a secondary environmental cause. We present four cases (1 man, 3 women) with an adult onset tic disorder (mean age of onset, 36 years; range, 27-42 years) associated with the presence of serum antibasal ganglia antibodies (ABGA). One patient had motor tics and unusual motor stereotypies, 2 had multiple motor and vocal tics, and the remaining patient had motor tics only. Concomitant psychiatric disturbance was noted in 3 cases. In 2 cases, there was a close temporal relationship between upper respiratory tract infection and the subsequent onset of tics. Imaging was possible in three cases and was normal in two but revealed a lesion involving the right caudate and lentiform nuclei in the other. We suggest that there might be a causal relationship between ABGA and the clinical syndrome in these cases and that ABGA should be considered as a possible etiology for adult-onset tics.
CC : 002B17; 002B17G; 002B17F
FD : Système nerveux pathologie; Stéréotypie; Tic; Trouble moteur; Contrôle moteur
FG : Mouvement involontaire; Trouble neurologique
ED : Nervous system diseases; Stereotypy; Tic; Motor system disorder; Motor control
EG : Involuntary movement; Neurological disorder
SD : Sistema nervioso patología; Estereotipia; Tic; Trastorno motor; Control motor
LO : INIST-20953.354000122474340090
ID : 04-0581920

Links to Exploration step

Pascal:04-0581920

Le document en format XML

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<div type="abstract" xml:lang="en">The onset of tics in adulthood is rare and, unlike the childhood variety, there is commonly a secondary environmental cause. We present four cases (1 man, 3 women) with an adult onset tic disorder (mean age of onset, 36 years; range, 27-42 years) associated with the presence of serum antibasal ganglia antibodies (ABGA). One patient had motor tics and unusual motor stereotypies, 2 had multiple motor and vocal tics, and the remaining patient had motor tics only. Concomitant psychiatric disturbance was noted in 3 cases. In 2 cases, there was a close temporal relationship between upper respiratory tract infection and the subsequent onset of tics. Imaging was possible in three cases and was normal in two but revealed a lesion involving the right caudate and lentiform nuclei in the other. We suggest that there might be a causal relationship between ABGA and the clinical syndrome in these cases and that ABGA should be considered as a possible etiology for adult-onset tics.</div>
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<s0>The onset of tics in adulthood is rare and, unlike the childhood variety, there is commonly a secondary environmental cause. We present four cases (1 man, 3 women) with an adult onset tic disorder (mean age of onset, 36 years; range, 27-42 years) associated with the presence of serum antibasal ganglia antibodies (ABGA). One patient had motor tics and unusual motor stereotypies, 2 had multiple motor and vocal tics, and the remaining patient had motor tics only. Concomitant psychiatric disturbance was noted in 3 cases. In 2 cases, there was a close temporal relationship between upper respiratory tract infection and the subsequent onset of tics. Imaging was possible in three cases and was normal in two but revealed a lesion involving the right caudate and lentiform nuclei in the other. We suggest that there might be a causal relationship between ABGA and the clinical syndrome in these cases and that ABGA should be considered as a possible etiology for adult-onset tics.</s0>
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<s0>002B17F</s0>
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<s5>01</s5>
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<s5>01</s5>
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</fC03>
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<s0>Tic</s0>
<s5>04</s5>
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<fC03 i1="03" i2="X" l="SPA">
<s0>Tic</s0>
<s5>04</s5>
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<s0>Trouble moteur</s0>
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<s5>07</s5>
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<s0>Trastorno motor</s0>
<s5>07</s5>
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<s0>Contrôle moteur</s0>
<s5>25</s5>
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<s5>25</s5>
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<s5>37</s5>
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<s5>38</s5>
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<s0>Neurological disorder</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Trastorno neurológico</s0>
<s5>38</s5>
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<fN21>
<s1>334</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
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<NO>PASCAL 04-0581920 INIST</NO>
<ET>Adult-onset tic disorder, motor stereotypies, and behavioural disturbance associated with antibasal ganglia antibodies</ET>
<AU>EDWARDS (Mark J.); DALE (Russell C.); CHURCH (Andrew J.); TRIKOULI (Eleni); QUINN (Niall P.); LEES (Andrew J.); GIOVANNONI (Gavin); BHATIA (Kailash P.)</AU>
<AF>Sobell Department of Movement Neuroscience and Movement Disorders, Institute of Neurology, University College London, Queen Square/London/Royaume-Uni (1 aut., 4 aut., 5 aut., 8 aut.); Neuroimmunology unit, Department of Neuroinflammation. Institute of Neurology, University College London, Queen Square/London/Royaume-Uni (2 aut., 3 aut., 7 aut.); Neurosciences unit, Institute of Child Health./London/Royaume-Uni (2 aut.); The Reta Lila Weston Institute of Neurological Studies, The Windeyer Building/London/Royaume-Uni (6 aut.)</AF>
<DT>Publication en série; Courte communication, note brève; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2004; Vol. 19; No. 10; Pp. 1190-1196; Bibl. 33 ref.</SO>
<LA>Anglais</LA>
<EA>The onset of tics in adulthood is rare and, unlike the childhood variety, there is commonly a secondary environmental cause. We present four cases (1 man, 3 women) with an adult onset tic disorder (mean age of onset, 36 years; range, 27-42 years) associated with the presence of serum antibasal ganglia antibodies (ABGA). One patient had motor tics and unusual motor stereotypies, 2 had multiple motor and vocal tics, and the remaining patient had motor tics only. Concomitant psychiatric disturbance was noted in 3 cases. In 2 cases, there was a close temporal relationship between upper respiratory tract infection and the subsequent onset of tics. Imaging was possible in three cases and was normal in two but revealed a lesion involving the right caudate and lentiform nuclei in the other. We suggest that there might be a causal relationship between ABGA and the clinical syndrome in these cases and that ABGA should be considered as a possible etiology for adult-onset tics.</EA>
<CC>002B17; 002B17G; 002B17F</CC>
<FD>Système nerveux pathologie; Stéréotypie; Tic; Trouble moteur; Contrôle moteur</FD>
<FG>Mouvement involontaire; Trouble neurologique</FG>
<ED>Nervous system diseases; Stereotypy; Tic; Motor system disorder; Motor control</ED>
<EG>Involuntary movement; Neurological disorder</EG>
<SD>Sistema nervioso patología; Estereotipia; Tic; Trastorno motor; Control motor</SD>
<LO>INIST-20953.354000122474340090</LO>
<ID>04-0581920</ID>
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