JankovicV1, PascalFrancis, Corpus, bibRecord, 000056

Hereditary chin tremor in Parkinson's disease

Identifieur interne : 000056 ( PascalFrancis/Corpus ); précédent : 000055; suivant : 000057

Hereditary chin tremor in Parkinson's disease

Auteurs : Sevda Erer ; Joseph Jankovic

Source :

Clinical neurology and neurosurgery [ 0303-8467 ] ; 2007.

RBID : Pascal:07-0457473

Descripteurs français

Pascal (Inist)
- Système nerveux pathologie, Tremblement, Parkinson maladie, Mouvement involontaire, Myoclonie, Chirurgie, Menton, Bontoxilysin.

English descriptors

KwdEn :
- Bontoxilysin, Chin, Involuntary movement, Myoclonus, Nervous system diseases, Parkinson disease, Surgery, Tremor.

Abstract

Hereditary chin tremor (HCT) is characterized by rhythmical, involuntary movements of the chin muscles usually inherited in an autosomal dominant pattern. We describe a 74-year old man with familial, childhood-onset chin tremor, and a 3-year history of progressive hand tremor, gait difficulty, and other parkinsonian features. Since chin tremor often occurs in Parkinson's disease (PD), a coexistent HCT may not be recognized unless past and family history of tremor is carefully explored.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A08	`01`	`1`	`ENG`	`@1 Hereditary chin tremor in Parkinson's disease`
A11	`01`	`1`		`@1 ERER (Sevda)`
A11	`02`	`1`		`@1 JANKOVIC (Joseph)`
A14	`01`			`@1 Parkinson's Disease Center and Movement Disorders Clinic, Department of Neurology, Baylor College of Medicine @2 Houston, Texas @3 USA @Z 1 aut. @Z 2 aut.`
A20				`@1 784-785`
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C01	`01`		`ENG`	`@0 Hereditary chin tremor (HCT) is characterized by rhythmical, involuntary movements of the chin muscles usually inherited in an autosomal dominant pattern. We describe a 74-year old man with familial, childhood-onset chin tremor, and a 3-year history of progressive hand tremor, gait difficulty, and other parkinsonian features. Since chin tremor often occurs in Parkinson's disease (PD), a coexistent HCT may not be recognized unless past and family history of tremor is carefully explored.`
C02	`01`	`X`		`@0 002B25J`
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 Tremblement @5 02`
C03	`02`	`X`	`ENG`	`@0 Tremor @5 02`
C03	`02`	`X`	`SPA`	`@0 Temblor @5 02`
C03	`03`	`X`	`FRE`	`@0 Parkinson maladie @5 03`
C03	`03`	`X`	`ENG`	`@0 Parkinson disease @5 03`
C03	`03`	`X`	`SPA`	`@0 Parkinson enfermedad @5 03`
C03	`04`	`X`	`FRE`	`@0 Mouvement involontaire @5 04`
C03	`04`	`X`	`ENG`	`@0 Involuntary movement @5 04`
C03	`04`	`X`	`SPA`	`@0 Movimiento involuntario @5 04`
C03	`05`	`X`	`FRE`	`@0 Myoclonie @5 05`
C03	`05`	`X`	`ENG`	`@0 Myoclonus @5 05`
C03	`05`	`X`	`SPA`	`@0 Mioclonia @5 05`
C03	`06`	`X`	`FRE`	`@0 Chirurgie @5 09`
C03	`06`	`X`	`ENG`	`@0 Surgery @5 09`
C03	`06`	`X`	`SPA`	`@0 Cirugía @5 09`
C03	`07`	`X`	`FRE`	`@0 Menton @5 10`
C03	`07`	`X`	`ENG`	`@0 Chin @5 10`
C03	`07`	`X`	`SPA`	`@0 Mentón @5 10`
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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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Format Inist (serveur)

NO :	PASCAL 07-0457473 INIST
ET :	Hereditary chin tremor in Parkinson's disease
AU :	ERER (Sevda); JANKOVIC (Joseph)
AF :	Parkinson's Disease Center and Movement Disorders Clinic, Department of Neurology, Baylor College of Medicine/Houston, Texas/Etats-Unis (1 aut., 2 aut.)
DT :	Publication en série; Etude de cas, cas et faits cliniques; Niveau analytique
SO :	Clinical neurology and neurosurgery; ISSN 0303-8467; Coden CNNSBV; Pays-Bas; Da. 2007; Vol. 109; No. 9; Pp. 784-785; Bibl. 14 ref.
LA :	Anglais
EA :	Hereditary chin tremor (HCT) is characterized by rhythmical, involuntary movements of the chin muscles usually inherited in an autosomal dominant pattern. We describe a 74-year old man with familial, childhood-onset chin tremor, and a 3-year history of progressive hand tremor, gait difficulty, and other parkinsonian features. Since chin tremor often occurs in Parkinson's disease (PD), a coexistent HCT may not be recognized unless past and family history of tremor is carefully explored.
CC :	002B25J
FD :	Système nerveux pathologie; Tremblement; Parkinson maladie; Mouvement involontaire; Myoclonie; Chirurgie; Menton; Bontoxilysin
FG :	Metalloendopeptidases; Peptidases; Hydrolases; Enzyme; Trouble neurologique; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Système nerveux central pathologie
ED :	Nervous system diseases; Tremor; Parkinson disease; Involuntary movement; Myoclonus; Surgery; Chin; Bontoxilysin
EG :	Metalloendopeptidases; Peptidases; Hydrolases; Enzyme; Neurological disorder; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease
SD :	Sistema nervioso patología; Temblor; Parkinson enfermedad; Movimiento involuntario; Mioclonia; Cirugía; Mentón; Bontoxilysin
LO :	INIST-4348.354000162535370090
ID :	07-0457473

Links to Exploration step

Pascal:07-0457473

Le document en format XML

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<front><div type="abstract" xml:lang="en">Hereditary chin tremor (HCT) is characterized by rhythmical, involuntary movements of the chin muscles usually inherited in an autosomal dominant pattern. We describe a 74-year old man with familial, childhood-onset chin tremor, and a 3-year history of progressive hand tremor, gait difficulty, and other parkinsonian features. Since chin tremor often occurs in Parkinson's disease (PD), a coexistent HCT may not be recognized unless past and family history of tremor is carefully explored.</div>
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<server><NO>PASCAL 07-0457473 INIST</NO>
<ET>Hereditary chin tremor in Parkinson's disease</ET>
<AU>ERER (Sevda); JANKOVIC (Joseph)</AU>
<AF>Parkinson's Disease Center and Movement Disorders Clinic, Department of Neurology, Baylor College of Medicine/Houston, Texas/Etats-Unis (1 aut., 2 aut.)</AF>
<DT>Publication en série; Etude de cas, cas et faits cliniques; Niveau analytique</DT>
<SO>Clinical neurology and neurosurgery; ISSN 0303-8467; Coden CNNSBV; Pays-Bas; Da. 2007; Vol. 109; No. 9; Pp. 784-785; Bibl. 14 ref.</SO>
<LA>Anglais</LA>
<EA>Hereditary chin tremor (HCT) is characterized by rhythmical, involuntary movements of the chin muscles usually inherited in an autosomal dominant pattern. We describe a 74-year old man with familial, childhood-onset chin tremor, and a 3-year history of progressive hand tremor, gait difficulty, and other parkinsonian features. Since chin tremor often occurs in Parkinson's disease (PD), a coexistent HCT may not be recognized unless past and family history of tremor is carefully explored.</EA>
<CC>002B25J</CC>
<FD>Système nerveux pathologie; Tremblement; Parkinson maladie; Mouvement involontaire; Myoclonie; Chirurgie; Menton; Bontoxilysin</FD>
<FG>Metalloendopeptidases; Peptidases; Hydrolases; Enzyme; Trouble neurologique; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Système nerveux central pathologie</FG>
<ED>Nervous system diseases; Tremor; Parkinson disease; Involuntary movement; Myoclonus; Surgery; Chin; Bontoxilysin</ED>
<EG>Metalloendopeptidases; Peptidases; Hydrolases; Enzyme; Neurological disorder; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease</EG>
<SD>Sistema nervioso patología; Temblor; Parkinson enfermedad; Movimiento involuntario; Mioclonia; Cirugía; Mentón; Bontoxilysin</SD>
<LO>INIST-4348.354000162535370090</LO>
<ID>07-0457473</ID>
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Hereditary chin tremor in Parkinson's disease

Hereditary chin tremor in Parkinson's disease

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