Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force.
Identifieur interne : 000216 ( Main/Merge ); précédent : 000215; suivant : 000217Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force.
Auteurs : Connie Marras [Canada] ; Anthony Lang [Canada] ; Bart P. Van De Warrenburg [Pays-Bas] ; Carolyn M. Sue [Australie] ; Sarah J. Tabrizi [Royaume-Uni] ; Lars Bertram [Allemagne] ; Saadet Mercimek-Mahmutoglu [Canada] ; Darius Ebrahimi-Fakhari [Allemagne] ; Thomas T. Warner [Royaume-Uni] ; Alexandra Durr [France] ; Birgit Assmann ; Katja Lohmann [Allemagne] ; Vladimir Kostic [Serbie] ; Christine Klein [Allemagne]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2016.
English descriptors
- KwdEn :
- MESH :
- classification : Movement Disorders.
- genetics : Movement Disorders.
- standards : Societies, Medical.
- Humans.
Abstract
The system of assigning locus symbols to specify chromosomal regions that are associated with a familial disorder has a number of problems when used as a reference list of genetically determined disorders,including (I) erroneously assigned loci, (II) duplicated loci, (III) missing symbols or loci, (IV) unconfirmed loci and genes, (V) a combination of causative genes and risk factor genes in the same list, and (VI) discordance between phenotype and list assignment. In this article, we report on the recommendations of the International Parkinson and Movement Disorder Society Task Force for Nomenclature of Genetic Movement Disorders and present a system for naming genetically determined movement disorders that addresses these problems. We demonstrate how the system would be applied to currently known genetically determined parkinsonism, dystonia, dominantly inherited ataxia, spastic paraparesis, chorea, paroxysmal movement disorders, neurodegeneration with brain iron accumulation, and primary familial brain calcifications. This system provides a resource for clinicians and researchers that, unlike the previous system, can be considered an accurate and criterion-based list of confirmed genetically determined movement disorders at the time it was last updated.
DOI: 10.1002/mds.26527
PubMed: 27079681
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pubmed:27079681Le document en format XML
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<front><div type="abstract" xml:lang="en">The system of assigning locus symbols to specify chromosomal regions that are associated with a familial disorder has a number of problems when used as a reference list of genetically determined disorders,including (I) erroneously assigned loci, (II) duplicated loci, (III) missing symbols or loci, (IV) unconfirmed loci and genes, (V) a combination of causative genes and risk factor genes in the same list, and (VI) discordance between phenotype and list assignment. In this article, we report on the recommendations of the International Parkinson and Movement Disorder Society Task Force for Nomenclature of Genetic Movement Disorders and present a system for naming genetically determined movement disorders that addresses these problems. We demonstrate how the system would be applied to currently known genetically determined parkinsonism, dystonia, dominantly inherited ataxia, spastic paraparesis, chorea, paroxysmal movement disorders, neurodegeneration with brain iron accumulation, and primary familial brain calcifications. This system provides a resource for clinicians and researchers that, unlike the previous system, can be considered an accurate and criterion-based list of confirmed genetically determined movement disorders at the time it was last updated.</div>
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