Diagnostic considerations in juvenile parkinsonism
Identifieur interne : 003D46 ( Main/Exploration ); précédent : 003D45; suivant : 003D47Diagnostic considerations in juvenile parkinsonism
Auteurs : Dominic C. Paviour [Royaume-Uni] ; Robert A. H. Surtees [Royaume-Uni] ; Andrew Lees (neurologue) [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 2004-02.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Adolescent, Adult, Brain (pathology), Chromosome Aberrations, Diagnosis, Genes, Recessive (genetics), Humans, Lewy Bodies (pathology), Mutation (genetics), Nervous system diseases, Neurologic Examination, Parkinson Disease (diagnosis), Parkinson Disease (genetics), Parkinson Disease (pathology), Parkinsonian Disorders (diagnosis), Parkinsonian Disorders (genetics), Parkinsonian Disorders (pathology), Parkinsonism, Ubiquitin-Protein Ligases (genetics), juvenile parkinsonism, parkin.
- MESH :
- chemical , genetics : Ubiquitin-Protein Ligases.
- diagnosis : Parkinson Disease, Parkinsonian Disorders.
- genetics : Genes, Recessive, Mutation, Parkinson Disease, Parkinsonian Disorders.
- pathology : Brain, Lewy Bodies, Parkinson Disease, Parkinsonian Disorders.
- Adolescent, Adult, Chromosome Aberrations, Humans, Neurologic Examination.
Abstract
Juvenile parkinsonism (JP) describes patients in whom the clinical features of parkinsonism manifest before 21 years of age. Many reported cases that had a good response to levodopa have proved to have autosomal recessive juvenile parkinsonism (AR‐JP) due to mutations in the parkin gene. With the exception of parkin mutations and dopa‐responsive dystonia, most causes are associated with the presence of additional neurological signs, resulting from additional lesions outside of the basal ganglia. Lewy body pathology has only been reported in one case, suggesting that a juvenile form of idiopathic Parkinson's disease may be extremely rare. © 2003 Movement Disorder Society
Url:
DOI: 10.1002/mds.10644
Affiliations:
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Le document en format XML
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<term>Diagnosis</term>
<term>Genes, Recessive (genetics)</term>
<term>Humans</term>
<term>Lewy Bodies (pathology)</term>
<term>Mutation (genetics)</term>
<term>Nervous system diseases</term>
<term>Neurologic Examination</term>
<term>Parkinson Disease (diagnosis)</term>
<term>Parkinson Disease (genetics)</term>
<term>Parkinson Disease (pathology)</term>
<term>Parkinsonian Disorders (diagnosis)</term>
<term>Parkinsonian Disorders (genetics)</term>
<term>Parkinsonian Disorders (pathology)</term>
<term>Parkinsonism</term>
<term>Ubiquitin-Protein Ligases (genetics)</term>
<term>juvenile parkinsonism</term>
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<term>Parkinsonian Disorders</term>
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<term>Mutation</term>
<term>Parkinson Disease</term>
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<term>Parkinsonian Disorders</term>
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<term>Neurologic Examination</term>
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<front><div type="abstract" xml:lang="en">Juvenile parkinsonism (JP) describes patients in whom the clinical features of parkinsonism manifest before 21 years of age. Many reported cases that had a good response to levodopa have proved to have autosomal recessive juvenile parkinsonism (AR‐JP) due to mutations in the parkin gene. With the exception of parkin mutations and dopa‐responsive dystonia, most causes are associated with the presence of additional neurological signs, resulting from additional lesions outside of the basal ganglia. Lewy body pathology has only been reported in one case, suggesting that a juvenile form of idiopathic Parkinson's disease may be extremely rare. © 2003 Movement Disorder Society</div>
</front>
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<name sortKey="Surtees, Robert A H" sort="Surtees, Robert A H" uniqKey="Surtees R" first="Robert A. H." last="Surtees">Robert A. H. Surtees</name>
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