Genetics of movement disorders.
Identifieur interne : 004480 ( Main/Curation ); précédent : 004479; suivant : 004481Genetics of movement disorders.
Auteurs : A. Dürr [France] ; A. BriceSource :
- Current opinion in neurology [ 1350-7540 ] ; 1996.
English descriptors
- KwdEn :
- Chromosome Aberrations (genetics), Chromosome Disorders, DNA Mutational Analysis, Genotype, Humans, Movement Disorders (classification), Movement Disorders (diagnosis), Movement Disorders (genetics), Parkinson Disease, Secondary (classification), Parkinson Disease, Secondary (diagnosis), Parkinson Disease, Secondary (genetics), Phenotype, Spinocerebellar Degenerations (classification), Spinocerebellar Degenerations (diagnosis), Spinocerebellar Degenerations (genetics), Trinucleotide Repeats (genetics).
- MESH :
- classification : Movement Disorders, Parkinson Disease, Secondary, Spinocerebellar Degenerations.
- diagnosis : Movement Disorders, Parkinson Disease, Secondary, Spinocerebellar Degenerations.
- genetics : Chromosome Aberrations, Movement Disorders, Parkinson Disease, Secondary, Spinocerebellar Degenerations, Trinucleotide Repeats.
- Chromosome Disorders, DNA Mutational Analysis, Genotype, Humans, Phenotype.
Abstract
Trinucleotide repeat expansions or unstable mutations are the cause of a growing number of hereditary movement disorders, especially inherited ataxias. Diagnostic practice as well as disease classifications have altered accordingly. Genes responsible for "Parkinsonian plus' syndromes and episodic movement disorders have also been recently mapped.
PubMed: 8858187
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pubmed:8858187Le document en format XML
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<term>Humans</term>
<term>Movement Disorders (classification)</term>
<term>Movement Disorders (diagnosis)</term>
<term>Movement Disorders (genetics)</term>
<term>Parkinson Disease, Secondary (classification)</term>
<term>Parkinson Disease, Secondary (diagnosis)</term>
<term>Parkinson Disease, Secondary (genetics)</term>
<term>Phenotype</term>
<term>Spinocerebellar Degenerations (classification)</term>
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<term>Trinucleotide Repeats (genetics)</term>
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<term>Parkinson Disease, Secondary</term>
<term>Spinocerebellar Degenerations</term>
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<term>Trinucleotide Repeats</term>
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<front><div type="abstract" xml:lang="en">Trinucleotide repeat expansions or unstable mutations are the cause of a growing number of hereditary movement disorders, especially inherited ataxias. Diagnostic practice as well as disease classifications have altered accordingly. Genes responsible for "Parkinsonian plus' syndromes and episodic movement disorders have also been recently mapped.</div>
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