Hereditary chin tremor in Parkinson's disease
Identifieur interne : 000E72 ( Main/Exploration ); précédent : 000E71; suivant : 000E73Hereditary chin tremor in Parkinson's disease
Auteurs : Sevda Erer [États-Unis] ; Joseph Jankovic [États-Unis]Source :
- Clinical neurology and neurosurgery [ 0303-8467 ] ; 2007.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Chirurgie.
English descriptors
- KwdEn :
- Aged, Antiparkinson Agents (therapeutic use), Bontoxilysin, Chin, Essential Tremor (complications), Essential Tremor (diagnosis), Essential Tremor (genetics), Humans, Involuntary movement, Male, Myoclonus, Nervous system diseases, Parkinson Disease (complications), Parkinson Disease (diagnosis), Parkinson Disease (drug therapy), Parkinson disease, Surgery, Tremor, Tremor (diagnosis), Tremor (drug therapy), Tremor (etiology).
- MESH :
- chemical , therapeutic use : Antiparkinson Agents.
- complications : Essential Tremor, Parkinson Disease.
- diagnosis : Essential Tremor, Parkinson Disease, Tremor.
- drug therapy : Parkinson Disease, Tremor.
- etiology : Tremor.
- genetics : Essential Tremor.
- Aged, Chin, Humans, Male.
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.
Affiliations:
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Le document en format XML
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<term>Antiparkinson Agents (therapeutic use)</term>
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<term>Chin</term>
<term>Essential Tremor (complications)</term>
<term>Essential Tremor (diagnosis)</term>
<term>Essential Tremor (genetics)</term>
<term>Humans</term>
<term>Involuntary movement</term>
<term>Male</term>
<term>Myoclonus</term>
<term>Nervous system diseases</term>
<term>Parkinson Disease (complications)</term>
<term>Parkinson Disease (diagnosis)</term>
<term>Parkinson Disease (drug therapy)</term>
<term>Parkinson disease</term>
<term>Surgery</term>
<term>Tremor</term>
<term>Tremor (diagnosis)</term>
<term>Tremor (drug therapy)</term>
<term>Tremor (etiology)</term>
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<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Essential Tremor</term>
<term>Parkinson Disease</term>
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<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Essential Tremor</term>
<term>Parkinson Disease</term>
<term>Tremor</term>
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<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Parkinson Disease</term>
<term>Tremor</term>
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<term>Chin</term>
<term>Humans</term>
<term>Male</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Système nerveux pathologie</term>
<term>Tremblement</term>
<term>Parkinson maladie</term>
<term>Mouvement involontaire</term>
<term>Myoclonie</term>
<term>Chirurgie</term>
<term>Menton</term>
<term>Bontoxilysin</term>
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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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<settlement><li>Houston</li>
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<orgName><li>Baylor College of Medicine</li>
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<name sortKey="Jankovic, Joseph" sort="Jankovic, Joseph" uniqKey="Jankovic J" first="Joseph" last="Jankovic">Joseph Jankovic</name>
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