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Movement Disorders (revue)

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Asynchronous blepharospasm, facial and cervical dystonia, and bilateral asynchronous hemifacial spasm

Identifieur interne : 001803 ( PascalFrancis/Corpus ); précédent : 001802; suivant : 001804

Asynchronous blepharospasm, facial and cervical dystonia, and bilateral asynchronous hemifacial spasm

Auteurs : Bradley J. Katz ; John R. Burroughs ; Richard L. Anderson ; Shannon Bownds ; John D. Mccann

Source :

RBID : Pascal:07-0133249

Descripteurs français

English descriptors

Abstract

We present a patient with a facial movement disorder that has characteristics of both blepharospasm and bilateral asynchronous hemifacial spasm. Because of the increased incidence of blepharospasm in patients with hemifacial spasm, our patient's clinical presentation is probably not a chance occurrence, but rather a manifestation of some predisposition for these two movement disorders. This unusual constellation of signs and symptoms challenges the current diagnostic criteria and suggests that some of these facial movement disorders may lie on a spectrum, rather than represent distinct entities.

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 22
A06       @2 2
A08 01  1  ENG  @1 Asynchronous blepharospasm, facial and cervical dystonia, and bilateral asynchronous hemifacial spasm
A11 01  1    @1 KATZ (Bradley J.)
A11 02  1    @1 BURROUGHS (John R.)
A11 03  1    @1 ANDERSON (Richard L.)
A11 04  1    @1 BOWNDS (Shannon)
A11 05  1    @1 MCCANN (John D.)
A14 01      @1 John A. Moran Eye Center, University of Utah Health Sciences Center @2 Salt Lake City, Utah @3 USA @Z 1 aut.
A14 02      @1 Department of Ophthalmology, University of Utah Health Sciences Center @2 Salt Lake City, Utah @3 USA @Z 1 aut.
A14 03      @1 Department of Neurology, University of Utah Health Sciences Center @2 Salt Lake City, Utah @3 USA @Z 1 aut.
A14 04      @1 Center for Facial Appearances @2 Salt Lake City, Utah @3 USA @Z 2 aut. @Z 3 aut. @Z 5 aut.
A14 05      @1 Department of Radiology, University of Utah Health Sciences Center @2 Salt Lake City, Utah @3 USA @Z 4 aut.
A20       @1 231-234
A21       @1 2007
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000145528070140
A44       @0 0000 @1 © 2007 INIST-CNRS. All rights reserved.
A45       @0 8 ref.
A47 01  1    @0 07-0133249
A60       @1 P @3 CC
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 We present a patient with a facial movement disorder that has characteristics of both blepharospasm and bilateral asynchronous hemifacial spasm. Because of the increased incidence of blepharospasm in patients with hemifacial spasm, our patient's clinical presentation is probably not a chance occurrence, but rather a manifestation of some predisposition for these two movement disorders. This unusual constellation of signs and symptoms challenges the current diagnostic criteria and suggests that some of these facial movement disorders may lie on a spectrum, rather than represent distinct entities.
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C02 03  X    @0 002B25I
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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 Blépharospasme @5 02
C03 02  X  ENG  @0 Blepharospasm @5 02
C03 02  X  SPA  @0 Blefaroespasmo @5 02
C03 03  X  FRE  @0 Dystonie @5 03
C03 03  X  ENG  @0 Dystonia @5 03
C03 03  X  SPA  @0 Distonía @5 03
C03 04  X  FRE  @0 Hémispasme facial @5 04
C03 04  X  ENG  @0 Hemifacial spasm @5 04
C03 04  X  SPA  @0 Hemiespasmo facial @5 04
C03 05  X  FRE  @0 Apraxie @5 05
C03 05  X  ENG  @0 Apraxia @5 05
C03 05  X  SPA  @0 Apraxia @5 05
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C03 06  X  ENG  @0 Meige syndrome @5 06
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C03 07  X  ENG  @0 Bontoxilysin @2 FE @2 FR @5 09
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C07 04  X  FRE  @0 Enzyme @2 FE
C07 04  X  ENG  @0 Enzyme @2 FE
C07 04  X  SPA  @0 Enzima @2 FE
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C07 05  X  ENG  @0 Eyelid disease @5 37
C07 05  X  SPA  @0 Párpado patología @5 37
C07 06  X  FRE  @0 Oeil pathologie @5 38
C07 06  X  ENG  @0 Eye disease @5 38
C07 06  X  SPA  @0 Ojo patología @5 38
C07 07  X  FRE  @0 Extrapyramidal syndrome @5 39
C07 07  X  ENG  @0 Extrapyramidal syndrome @5 39
C07 07  X  SPA  @0 Extrapiramidal síndrome @5 39
C07 08  X  FRE  @0 Mouvement involontaire @5 40
C07 08  X  ENG  @0 Involuntary movement @5 40
C07 08  X  SPA  @0 Movimiento involuntario @5 40
C07 09  X  FRE  @0 Muscle strié pathologie @5 41
C07 09  X  ENG  @0 Striated muscle disease @5 41
C07 09  X  SPA  @0 Músculo estriado patología @5 41
C07 10  X  FRE  @0 Trouble neurologique @5 42
C07 10  X  ENG  @0 Neurological disorder @5 42
C07 10  X  SPA  @0 Trastorno neurológico @5 42
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C07 11  X  ENG  @0 Cerebral disorder @5 43
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C07 12  X  FRE  @0 Système nerveux central pathologie @5 44
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Format Inist (serveur)

NO : PASCAL 07-0133249 INIST
ET : Asynchronous blepharospasm, facial and cervical dystonia, and bilateral asynchronous hemifacial spasm
AU : KATZ (Bradley J.); BURROUGHS (John R.); ANDERSON (Richard L.); BOWNDS (Shannon); MCCANN (John D.)
AF : John A. Moran Eye Center, University of Utah Health Sciences Center/Salt Lake City, Utah/Etats-Unis (1 aut.); Department of Ophthalmology, University of Utah Health Sciences Center/Salt Lake City, Utah/Etats-Unis (1 aut.); Department of Neurology, University of Utah Health Sciences Center/Salt Lake City, Utah/Etats-Unis (1 aut.); Center for Facial Appearances/Salt Lake City, Utah/Etats-Unis (2 aut., 3 aut., 5 aut.); Department of Radiology, University of Utah Health Sciences Center/Salt Lake City, Utah/Etats-Unis (4 aut.)
DT : Publication en série; Courte communication, note brève; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2007; Vol. 22; No. 2; Pp. 231-234; Bibl. 8 ref.
LA : Anglais
EA : We present a patient with a facial movement disorder that has characteristics of both blepharospasm and bilateral asynchronous hemifacial spasm. Because of the increased incidence of blepharospasm in patients with hemifacial spasm, our patient's clinical presentation is probably not a chance occurrence, but rather a manifestation of some predisposition for these two movement disorders. This unusual constellation of signs and symptoms challenges the current diagnostic criteria and suggests that some of these facial movement disorders may lie on a spectrum, rather than represent distinct entities.
CC : 002B17; 002B17H; 002B25I
FD : Système nerveux pathologie; Blépharospasme; Dystonie; Hémispasme facial; Apraxie; Meige syndrome; Bontoxilysin
FG : Metalloendopeptidases; Peptidases; Hydrolases; Enzyme; Paupière pathologie; Oeil pathologie; Extrapyramidal syndrome; Mouvement involontaire; Muscle strié pathologie; Trouble neurologique; Encéphale pathologie; Système nerveux central pathologie
ED : Nervous system diseases; Blepharospasm; Dystonia; Hemifacial spasm; Apraxia; Meige syndrome; Bontoxilysin
EG : Metalloendopeptidases; Peptidases; Hydrolases; Enzyme; Eyelid disease; Eye disease; Extrapyramidal syndrome; Involuntary movement; Striated muscle disease; Neurological disorder; Cerebral disorder; Central nervous system disease
SD : Sistema nervioso patología; Blefaroespasmo; Distonía; Hemiespasmo facial; Apraxia; Meige síndrome; Bontoxilysin
LO : INIST-20953.354000145528070140
ID : 07-0133249

Links to Exploration step

Pascal:07-0133249

Le document en format XML

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</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Hémispasme facial</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Hemifacial spasm</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Hemiespasmo facial</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Apraxie</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Apraxia</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Apraxia</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Meige syndrome</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Meige syndrome</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Meige síndrome</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Bontoxilysin</s0>
<s2>FE</s2>
<s2>FR</s2>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Bontoxilysin</s0>
<s2>FE</s2>
<s2>FR</s2>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Bontoxilysin</s0>
<s2>FE</s2>
<s2>FR</s2>
<s5>09</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Metalloendopeptidases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Metalloendopeptidases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Metalloendopeptidases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Peptidases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Peptidases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Peptidases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Enzima</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Paupière pathologie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Eyelid disease</s0>
<s5>37</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Párpado patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Oeil pathologie</s0>
<s5>38</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Eye disease</s0>
<s5>38</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Ojo patología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Extrapyramidal syndrome</s0>
<s5>39</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Extrapyramidal syndrome</s0>
<s5>39</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Extrapiramidal síndrome</s0>
<s5>39</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Mouvement involontaire</s0>
<s5>40</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Involuntary movement</s0>
<s5>40</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Movimiento involuntario</s0>
<s5>40</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE">
<s0>Muscle strié pathologie</s0>
<s5>41</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG">
<s0>Striated muscle disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA">
<s0>Músculo estriado patología</s0>
<s5>41</s5>
</fC07>
<fC07 i1="10" i2="X" l="FRE">
<s0>Trouble neurologique</s0>
<s5>42</s5>
</fC07>
<fC07 i1="10" i2="X" l="ENG">
<s0>Neurological disorder</s0>
<s5>42</s5>
</fC07>
<fC07 i1="10" i2="X" l="SPA">
<s0>Trastorno neurológico</s0>
<s5>42</s5>
</fC07>
<fC07 i1="11" i2="X" l="FRE">
<s0>Encéphale pathologie</s0>
<s5>43</s5>
</fC07>
<fC07 i1="11" i2="X" l="ENG">
<s0>Cerebral disorder</s0>
<s5>43</s5>
</fC07>
<fC07 i1="11" i2="X" l="SPA">
<s0>Encéfalo patología</s0>
<s5>43</s5>
</fC07>
<fC07 i1="12" i2="X" l="FRE">
<s0>Système nerveux central pathologie</s0>
<s5>44</s5>
</fC07>
<fC07 i1="12" i2="X" l="ENG">
<s0>Central nervous system disease</s0>
<s5>44</s5>
</fC07>
<fC07 i1="12" i2="X" l="SPA">
<s0>Sistema nervosio central patología</s0>
<s5>44</s5>
</fC07>
<fN21>
<s1>085</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 07-0133249 INIST</NO>
<ET>Asynchronous blepharospasm, facial and cervical dystonia, and bilateral asynchronous hemifacial spasm</ET>
<AU>KATZ (Bradley J.); BURROUGHS (John R.); ANDERSON (Richard L.); BOWNDS (Shannon); MCCANN (John D.)</AU>
<AF>John A. Moran Eye Center, University of Utah Health Sciences Center/Salt Lake City, Utah/Etats-Unis (1 aut.); Department of Ophthalmology, University of Utah Health Sciences Center/Salt Lake City, Utah/Etats-Unis (1 aut.); Department of Neurology, University of Utah Health Sciences Center/Salt Lake City, Utah/Etats-Unis (1 aut.); Center for Facial Appearances/Salt Lake City, Utah/Etats-Unis (2 aut., 3 aut., 5 aut.); Department of Radiology, University of Utah Health Sciences Center/Salt Lake City, Utah/Etats-Unis (4 aut.)</AF>
<DT>Publication en série; Courte communication, note brève; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2007; Vol. 22; No. 2; Pp. 231-234; Bibl. 8 ref.</SO>
<LA>Anglais</LA>
<EA>We present a patient with a facial movement disorder that has characteristics of both blepharospasm and bilateral asynchronous hemifacial spasm. Because of the increased incidence of blepharospasm in patients with hemifacial spasm, our patient's clinical presentation is probably not a chance occurrence, but rather a manifestation of some predisposition for these two movement disorders. This unusual constellation of signs and symptoms challenges the current diagnostic criteria and suggests that some of these facial movement disorders may lie on a spectrum, rather than represent distinct entities.</EA>
<CC>002B17; 002B17H; 002B25I</CC>
<FD>Système nerveux pathologie; Blépharospasme; Dystonie; Hémispasme facial; Apraxie; Meige syndrome; Bontoxilysin</FD>
<FG>Metalloendopeptidases; Peptidases; Hydrolases; Enzyme; Paupière pathologie; Oeil pathologie; Extrapyramidal syndrome; Mouvement involontaire; Muscle strié pathologie; Trouble neurologique; Encéphale pathologie; Système nerveux central pathologie</FG>
<ED>Nervous system diseases; Blepharospasm; Dystonia; Hemifacial spasm; Apraxia; Meige syndrome; Bontoxilysin</ED>
<EG>Metalloendopeptidases; Peptidases; Hydrolases; Enzyme; Eyelid disease; Eye disease; Extrapyramidal syndrome; Involuntary movement; Striated muscle disease; Neurological disorder; Cerebral disorder; Central nervous system disease</EG>
<SD>Sistema nervioso patología; Blefaroespasmo; Distonía; Hemiespasmo facial; Apraxia; Meige síndrome; Bontoxilysin</SD>
<LO>INIST-20953.354000145528070140</LO>
<ID>07-0133249</ID>
</server>
</inist>
</record>

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