Other causes of parkinsonism.
Identifieur interne : 001535 ( PubMed/Corpus ); précédent : 001534; suivant : 001536Other causes of parkinsonism.
Auteurs : F. TisonSource :
- Bailliere's clinical neurology [ 0961-0421 ] ; 1997.
English descriptors
- KwdEn :
- Antipsychotic Agents (adverse effects), Basal Ganglia (pathology), Cerebrovascular Disorders (complications), Communicable Diseases (complications), Craniocerebral Trauma (complications), Diagnosis, Differential, Humans, Hydrocephalus (complications), Metabolism, Inborn Errors (complications), Neurodegenerative Diseases (complications), Neurotoxins (adverse effects), Parkinson Disease, Secondary (chemically induced), Parkinson Disease, Secondary (diagnosis), Parkinson Disease, Secondary (etiology), Pedigree.
- MESH :
- chemical , adverse effects : Antipsychotic Agents, Neurotoxins.
- chemically induced : Parkinson Disease, Secondary.
- complications : Cerebrovascular Disorders, Communicable Diseases, Craniocerebral Trauma, Hydrocephalus, Metabolism, Inborn Errors, Neurodegenerative Diseases.
- diagnosis : Parkinson Disease, Secondary.
- etiology : Parkinson Disease, Secondary.
- pathology : Basal Ganglia.
- Diagnosis, Differential, Humans, Pedigree.
Abstract
This chapter deals with the 'other causes of parkinsonism with the exclusion of idiopathic Parkinson's disease, multiple system atrophy, progressive supranuclear palsy and corticobasal degeneration. It is a cursory glance over the endless list of 'secondary' causes of parkinsonism or parkinsonism due to acquired and inherited metabolic and neurodegenerative diseases. With the exception of drug-induced parkinsonism and 'vascular' parkinsonism, most such cases are rare. However, single rare causes must not be overlooked as there can be specific therapeutic consequences. Parkinsonism is often present amid a constellation of other symptoms. Careful evaluation of the personal, familial and environmental context, mode of onset and progression, clinical features, and drug response, together with imaging, biochemical and molecular tests, help in determining the underlying disease.
PubMed: 9426876
Links to Exploration step
pubmed:9426876Le document en format XML
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<term>Basal Ganglia (pathology)</term>
<term>Cerebrovascular Disorders (complications)</term>
<term>Communicable Diseases (complications)</term>
<term>Craniocerebral Trauma (complications)</term>
<term>Diagnosis, Differential</term>
<term>Humans</term>
<term>Hydrocephalus (complications)</term>
<term>Metabolism, Inborn Errors (complications)</term>
<term>Neurodegenerative Diseases (complications)</term>
<term>Neurotoxins (adverse effects)</term>
<term>Parkinson Disease, Secondary (chemically induced)</term>
<term>Parkinson Disease, Secondary (diagnosis)</term>
<term>Parkinson Disease, Secondary (etiology)</term>
<term>Pedigree</term>
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<keywords scheme="MESH" type="chemical" qualifier="adverse effects" xml:lang="en"><term>Antipsychotic Agents</term>
<term>Neurotoxins</term>
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<term>Communicable Diseases</term>
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<term>Metabolism, Inborn Errors</term>
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<front><div type="abstract" xml:lang="en">This chapter deals with the 'other causes of parkinsonism with the exclusion of idiopathic Parkinson's disease, multiple system atrophy, progressive supranuclear palsy and corticobasal degeneration. It is a cursory glance over the endless list of 'secondary' causes of parkinsonism or parkinsonism due to acquired and inherited metabolic and neurodegenerative diseases. With the exception of drug-induced parkinsonism and 'vascular' parkinsonism, most such cases are rare. However, single rare causes must not be overlooked as there can be specific therapeutic consequences. Parkinsonism is often present amid a constellation of other symptoms. Careful evaluation of the personal, familial and environmental context, mode of onset and progression, clinical features, and drug response, together with imaging, biochemical and molecular tests, help in determining the underlying disease.</div>
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<Title>Bailliere's clinical neurology</Title>
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<Abstract><AbstractText>This chapter deals with the 'other causes of parkinsonism with the exclusion of idiopathic Parkinson's disease, multiple system atrophy, progressive supranuclear palsy and corticobasal degeneration. It is a cursory glance over the endless list of 'secondary' causes of parkinsonism or parkinsonism due to acquired and inherited metabolic and neurodegenerative diseases. With the exception of drug-induced parkinsonism and 'vascular' parkinsonism, most such cases are rare. However, single rare causes must not be overlooked as there can be specific therapeutic consequences. Parkinsonism is often present amid a constellation of other symptoms. Careful evaluation of the personal, familial and environmental context, mode of onset and progression, clinical features, and drug response, together with imaging, biochemical and molecular tests, help in determining the underlying disease.</AbstractText>
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<NumberOfReferences>72</NumberOfReferences>
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