Hereditary chin tremor in Parkinson's disease
Identifieur interne : 000056 ( PascalFrancis/Corpus ); précédent : 000055; suivant : 000057Hereditary chin tremor in Parkinson's disease
Auteurs : Sevda Erer ; Joseph JankovicSource :
- Clinical neurology and neurosurgery [ 0303-8467 ] ; 2007.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
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.
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Pour connaître la documentation sur le format Inist Standard.
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Format Inist (serveur)
NO : | PASCAL 07-0457473 INIST |
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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 |
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Pascal:07-0457473Le 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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<ET>Hereditary chin tremor in Parkinson's disease</ET>
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<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>
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