MovDisordV3, PascalFrancis, Corpus, bibRecord, 001884

Neuropsychological profile of DYT1 dystonia

Identifieur interne : 001884 ( PascalFrancis/Corpus ); précédent : 001883; suivant : 001885

Neuropsychological profile of DYT1 dystonia

Auteurs : Meirav Balas ; Chava Peretz ; Samih Badarny ; Richard B. Scott ; Nir Giladi

Source :

Movement disorders [ 0885-3185 ] ; 2006.

RBID : Pascal:07-0090855

Descripteurs français

Pascal (Inist)
- Système nerveux pathologie, Dystonie, Fonction exécutive, Interférence.

English descriptors

KwdEn :
- Dystonia, Executive function, Interference, Nervous system diseases.

Abstract

The common belief that primary dystonia is a purely motor disorder has recently been challenged. We examined separately the cognitive profiles of symptomatic (SYM) and nonsymptomatic (N-SYM) groups of carriers of DYT1 mutation using a comprehensive neuropsychological test battery. Self-report inventories of anxiety, depression, and pain levels were also administered, as well as manual motor dexterity assessment. Each group was matched with healthy controls by age, sex, mother tongue, and education. No significant differences between the SYM group to its control group were found on cognitive tests evaluating verbal and nonverbal abstract abilities, attention, information processing speed, and spatial organization. However, the SYM group showed increased verbal memory retroactive interference. Interestingly, the patients also showed higher semantic fluency performance. No significant differences between the N-SYM group to controls were found. It was concluded that symptomatic DYT1 mutation carriers do not suffer the distinctive cognitive decline that is seen in other primary degenerative extrapyramidal disorders.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A03		`1`		`@0 Mov. disord.`
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A08	`01`	`1`	`ENG`	`@1 Neuropsychological profile of DYT1 dystonia`
A11	`01`	`1`		`@1 BALAS (Meirav)`
A11	`02`	`1`		`@1 PERETZ (Chava)`
A11	`03`	`1`		`@1 BADARNY (Samih)`
A11	`04`	`1`		`@1 SCOTT (Richard B.)`
A11	`05`	`1`		`@1 GILADI (Nir)`
A14	`01`			`@1 Movement Disorders Unit, Department of Neurology, Tel Aviv Sourasky Medical Center @2 Tel Aviv @3 ISR @Z 1 aut. @Z 2 aut. @Z 5 aut.`
A14	`02`			`@1 Brain Behavior Research Center, University of Haifa @2 Haifa @3 ISR @Z 1 aut.`
A14	`03`			`@1 Sackler School of Medicine, Tel Aviv University @2 Tel Aviv @3 ISR @Z 2 aut. @Z 5 aut.`
A14	`04`			`@1 Movement Disorders Clinic, Department of Neurology, Carmel Medical Center @2 Haifa @3 ISR @Z 3 aut.`
A14	`05`			`@1 Rappaport Faculty of Medicine, Technion, Israel Institute of Technology @2 Haifa @3 ISR @Z 3 aut.`
A14	`06`			`@1 Russell-Cairns Unit, Radcliffe Infirmary @2 Oxford @3 GBR @Z 4 aut.`
A20				`@1 2073-2077`
A21				`@1 2006`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000145356790050`
A44				`@0 0000 @1 © 2007 INIST-CNRS. All rights reserved.`
A45				`@0 25 ref.`
A47	`01`	`1`		`@0 07-0090855`
A60				`@1 P`
A61				`@0 A`
A64	`01`	`1`		`@0 Movement disorders`
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C01	`01`		`ENG`	@0 The common belief that primary dystonia is a purely motor disorder has recently been challenged. We examined separately the cognitive profiles of symptomatic (SYM) and nonsymptomatic (N-SYM) groups of carriers of DYT1 mutation using a comprehensive neuropsychological test battery. Self-report inventories of anxiety, depression, and pain levels were also administered, as well as manual motor dexterity assessment. Each group was matched with healthy controls by age, sex, mother tongue, and education. No significant differences between the SYM group to its control group were found on cognitive tests evaluating verbal and nonverbal abstract abilities, attention, information processing speed, and spatial organization. However, the SYM group showed increased verbal memory retroactive interference. Interestingly, the patients also showed higher semantic fluency performance. No significant differences between the N-SYM group to controls were found. It was concluded that symptomatic DYT1 mutation carriers do not suffer the distinctive cognitive decline that is seen in other primary degenerative extrapyramidal disorders.
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C03	`01`	`X`	`SPA`	`@0 Sistema nervioso patología @5 01`
C03	`02`	`X`	`FRE`	`@0 Dystonie @5 02`
C03	`02`	`X`	`ENG`	`@0 Dystonia @5 02`
C03	`02`	`X`	`SPA`	`@0 Distonía @5 02`
C03	`03`	`X`	`FRE`	`@0 Fonction exécutive @5 09`
C03	`03`	`X`	`ENG`	`@0 Executive function @5 09`
C03	`03`	`X`	`SPA`	`@0 Función ejecutiva @5 09`
C03	`04`	`X`	`FRE`	`@0 Interférence @5 10`
C03	`04`	`X`	`ENG`	`@0 Interference @5 10`
C03	`04`	`X`	`SPA`	`@0 Interferencia @5 10`
C07	`01`	`X`	`FRE`	`@0 Extrapyramidal syndrome @5 37`
C07	`01`	`X`	`ENG`	`@0 Extrapyramidal syndrome @5 37`
C07	`01`	`X`	`SPA`	`@0 Extrapiramidal síndrome @5 37`
C07	`02`	`X`	`FRE`	`@0 Mouvement involontaire @5 38`
C07	`02`	`X`	`ENG`	`@0 Involuntary movement @5 38`
C07	`02`	`X`	`SPA`	`@0 Movimiento involuntario @5 38`
C07	`03`	`X`	`FRE`	`@0 Muscle strié pathologie @5 39`
C07	`03`	`X`	`ENG`	`@0 Striated muscle disease @5 39`
C07	`03`	`X`	`SPA`	`@0 Músculo estriado patología @5 39`
C07	`04`	`X`	`FRE`	`@0 Trouble neurologique @5 40`
C07	`04`	`X`	`ENG`	`@0 Neurological disorder @5 40`
C07	`04`	`X`	`SPA`	`@0 Trastorno neurológico @5 40`
C07	`05`	`X`	`FRE`	`@0 Encéphale pathologie @5 41`
C07	`05`	`X`	`ENG`	`@0 Cerebral disorder @5 41`
C07	`05`	`X`	`SPA`	`@0 Encéfalo patología @5 41`
C07	`06`	`X`	`FRE`	`@0 Système nerveux central pathologie @5 42`
C07	`06`	`X`	`ENG`	`@0 Central nervous system disease @5 42`
C07	`06`	`X`	`SPA`	`@0 Sistema nervosio central patología @5 42`
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Format Inist (serveur)

NO :	PASCAL 07-0090855 INIST
ET :	Neuropsychological profile of DYT1 dystonia
AU :	BALAS (Meirav); PERETZ (Chava); BADARNY (Samih); SCOTT (Richard B.); GILADI (Nir)
AF :	Movement Disorders Unit, Department of Neurology, Tel Aviv Sourasky Medical Center/Tel Aviv/Israël (1 aut., 2 aut., 5 aut.); Brain Behavior Research Center, University of Haifa/Haifa/Israël (1 aut.); Sackler School of Medicine, Tel Aviv University/Tel Aviv/Israël (2 aut., 5 aut.); Movement Disorders Clinic, Department of Neurology, Carmel Medical Center/Haifa/Israël (3 aut.); Rappaport Faculty of Medicine, Technion, Israel Institute of Technology/Haifa/Israël (3 aut.); Russell-Cairns Unit, Radcliffe Infirmary/Oxford/Royaume-Uni (4 aut.)
DT :	Publication en série; Niveau analytique
SO :	Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2006; Vol. 21; No. 12; Pp. 2073-2077; Bibl. 25 ref.
LA :	Anglais
EA :	The common belief that primary dystonia is a purely motor disorder has recently been challenged. We examined separately the cognitive profiles of symptomatic (SYM) and nonsymptomatic (N-SYM) groups of carriers of DYT1 mutation using a comprehensive neuropsychological test battery. Self-report inventories of anxiety, depression, and pain levels were also administered, as well as manual motor dexterity assessment. Each group was matched with healthy controls by age, sex, mother tongue, and education. No significant differences between the SYM group to its control group were found on cognitive tests evaluating verbal and nonverbal abstract abilities, attention, information processing speed, and spatial organization. However, the SYM group showed increased verbal memory retroactive interference. Interestingly, the patients also showed higher semantic fluency performance. No significant differences between the N-SYM group to controls were found. It was concluded that symptomatic DYT1 mutation carriers do not suffer the distinctive cognitive decline that is seen in other primary degenerative extrapyramidal disorders.
CC :	002B17; 002B17H; 002B17F
FD :	Système nerveux pathologie; Dystonie; Fonction exécutive; Interférence
FG :	Extrapyramidal syndrome; Mouvement involontaire; Muscle strié pathologie; Trouble neurologique; Encéphale pathologie; Système nerveux central pathologie
ED :	Nervous system diseases; Dystonia; Executive function; Interference
EG :	Extrapyramidal syndrome; Involuntary movement; Striated muscle disease; Neurological disorder; Cerebral disorder; Central nervous system disease
SD :	Sistema nervioso patología; Distonía; Función ejecutiva; Interferencia
LO :	INIST-20953.354000145356790050
ID :	07-0090855

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Pascal:07-0090855

Le document en format XML

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<front><div type="abstract" xml:lang="en">The common belief that primary dystonia is a purely motor disorder has recently been challenged. We examined separately the cognitive profiles of symptomatic (SYM) and nonsymptomatic (N-SYM) groups of carriers of DYT1 mutation using a comprehensive neuropsychological test battery. Self-report inventories of anxiety, depression, and pain levels were also administered, as well as manual motor dexterity assessment. Each group was matched with healthy controls by age, sex, mother tongue, and education. No significant differences between the SYM group to its control group were found on cognitive tests evaluating verbal and nonverbal abstract abilities, attention, information processing speed, and spatial organization. However, the SYM group showed increased verbal memory retroactive interference. Interestingly, the patients also showed higher semantic fluency performance. No significant differences between the N-SYM group to controls were found. It was concluded that symptomatic DYT1 mutation carriers do not suffer the distinctive cognitive decline that is seen in other primary degenerative extrapyramidal disorders.</div>
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<fC01 i1="01" l="ENG"><s0>The common belief that primary dystonia is a purely motor disorder has recently been challenged. We examined separately the cognitive profiles of symptomatic (SYM) and nonsymptomatic (N-SYM) groups of carriers of DYT1 mutation using a comprehensive neuropsychological test battery. Self-report inventories of anxiety, depression, and pain levels were also administered, as well as manual motor dexterity assessment. Each group was matched with healthy controls by age, sex, mother tongue, and education. No significant differences between the SYM group to its control group were found on cognitive tests evaluating verbal and nonverbal abstract abilities, attention, information processing speed, and spatial organization. However, the SYM group showed increased verbal memory retroactive interference. Interestingly, the patients also showed higher semantic fluency performance. No significant differences between the N-SYM group to controls were found. It was concluded that symptomatic DYT1 mutation carriers do not suffer the distinctive cognitive decline that is seen in other primary degenerative extrapyramidal disorders.</s0>
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<fC03 i1="03" i2="X" l="ENG"><s0>Executive function</s0>
<s5>09</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Función ejecutiva</s0>
<s5>09</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Interférence</s0>
<s5>10</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Interference</s0>
<s5>10</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Interferencia</s0>
<s5>10</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Extrapyramidal syndrome</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Mouvement involontaire</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Involuntary movement</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Movimiento involuntario</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Muscle strié pathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Striated muscle disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Músculo estriado patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Trouble neurologique</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Neurological disorder</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Trastorno neurológico</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Encéphale pathologie</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Système nerveux central pathologie</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>42</s5>
</fC07>
<fN21><s1>057</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
<server><NO>PASCAL 07-0090855 INIST</NO>
<ET>Neuropsychological profile of DYT1 dystonia</ET>
<AU>BALAS (Meirav); PERETZ (Chava); BADARNY (Samih); SCOTT (Richard B.); GILADI (Nir)</AU>
<AF>Movement Disorders Unit, Department of Neurology, Tel Aviv Sourasky Medical Center/Tel Aviv/Israël (1 aut., 2 aut., 5 aut.); Brain Behavior Research Center, University of Haifa/Haifa/Israël (1 aut.); Sackler School of Medicine, Tel Aviv University/Tel Aviv/Israël (2 aut., 5 aut.); Movement Disorders Clinic, Department of Neurology, Carmel Medical Center/Haifa/Israël (3 aut.); Rappaport Faculty of Medicine, Technion, Israel Institute of Technology/Haifa/Israël (3 aut.); Russell-Cairns Unit, Radcliffe Infirmary/Oxford/Royaume-Uni (4 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2006; Vol. 21; No. 12; Pp. 2073-2077; Bibl. 25 ref.</SO>
<LA>Anglais</LA>
<EA>The common belief that primary dystonia is a purely motor disorder has recently been challenged. We examined separately the cognitive profiles of symptomatic (SYM) and nonsymptomatic (N-SYM) groups of carriers of DYT1 mutation using a comprehensive neuropsychological test battery. Self-report inventories of anxiety, depression, and pain levels were also administered, as well as manual motor dexterity assessment. Each group was matched with healthy controls by age, sex, mother tongue, and education. No significant differences between the SYM group to its control group were found on cognitive tests evaluating verbal and nonverbal abstract abilities, attention, information processing speed, and spatial organization. However, the SYM group showed increased verbal memory retroactive interference. Interestingly, the patients also showed higher semantic fluency performance. No significant differences between the N-SYM group to controls were found. It was concluded that symptomatic DYT1 mutation carriers do not suffer the distinctive cognitive decline that is seen in other primary degenerative extrapyramidal disorders.</EA>
<CC>002B17; 002B17H; 002B17F</CC>
<FD>Système nerveux pathologie; Dystonie; Fonction exécutive; Interférence</FD>
<FG>Extrapyramidal syndrome; Mouvement involontaire; Muscle strié pathologie; Trouble neurologique; Encéphale pathologie; Système nerveux central pathologie</FG>
<ED>Nervous system diseases; Dystonia; Executive function; Interference</ED>
<EG>Extrapyramidal syndrome; Involuntary movement; Striated muscle disease; Neurological disorder; Cerebral disorder; Central nervous system disease</EG>
<SD>Sistema nervioso patología; Distonía; Función ejecutiva; Interferencia</SD>
<LO>INIST-20953.354000145356790050</LO>
<ID>07-0090855</ID>
</server>
</inist>
</record>

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	Movement Disorders (revue)
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Movement Disorders (revue)

Neuropsychological profile of DYT1 dystonia

Neuropsychological profile of DYT1 dystonia

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