Screening for dystonia genes DYT1, 11 and 16 in patients with writer's cramp
Identifieur interne : 002923 ( Main/Merge ); précédent : 002922; suivant : 002924Screening for dystonia genes DYT1, 11 and 16 in patients with writer's cramp
Auteurs : Katja Ritz [Pays-Bas] ; Justus L. Groen [Pays-Bas] ; Jose J. M. Kruisdijk [Pays-Bas] ; Frank Baas [Pays-Bas] ; Johannes H. T. M. Koelman [Pays-Bas] ; Marina A. J. Tijssen [Pays-Bas]Source :
- Movement Disorders [ 0885-3185 ] ; 2009-07-15.
English descriptors
- KwdEn :
- Adolescent, Adult, Aged, DYT1, DYT11, DYT16, Dystonic Disorders (genetics), Female, Genetic Predisposition to Disease, Genetic Testing (methods), Genotype, Humans, Male, Middle Aged, Molecular Chaperones (genetics), Mutation (genetics), RNA-Binding Proteins (genetics), Sarcoglycans (genetics), Trinucleotide Repeat Expansion (genetics), Young Adult, writer's cramp.
- MESH :
- chemical , genetics : Molecular Chaperones, RNA-Binding Proteins, Sarcoglycans.
- genetics : Dystonic Disorders, Mutation, Trinucleotide Repeat Expansion.
- methods : Genetic Testing.
- Adolescent, Adult, Aged, Female, Genetic Predisposition to Disease, Genotype, Humans, Male, Middle Aged, Young Adult.
Abstract
Task‐specific focal upper limb dystonia can be part of the phenotypic spectrum of different types of hereditary dystonia. We investigated whether writer's cramp as presenting symptom is associated with mutations in DYT11, DYT16, or with the DYT1 GAG deletion in 43 patients. No DYT11 and DYT16 mutations were identified. One patient carried the GAG deletion in the DYT1 gene. In our cohort, writer's cramp as presenting symptom is not associated with mutations in DYT11, DYT16, but it can be the sole manifestation of DYT1 GAG deletion mutation carriers. © 2009 Movement Disorder Society
Url:
DOI: 10.1002/mds.22632
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<front><div type="abstract" xml:lang="en">Task‐specific focal upper limb dystonia can be part of the phenotypic spectrum of different types of hereditary dystonia. We investigated whether writer's cramp as presenting symptom is associated with mutations in DYT11, DYT16, or with the DYT1 GAG deletion in 43 patients. No DYT11 and DYT16 mutations were identified. One patient carried the GAG deletion in the DYT1 gene. In our cohort, writer's cramp as presenting symptom is not associated with mutations in DYT11, DYT16, but it can be the sole manifestation of DYT1 GAG deletion mutation carriers. © 2009 Movement Disorder Society</div>
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<term>Female</term>
<term>Genetic Predisposition to Disease</term>
<term>Genetic Testing (methods)</term>
<term>Genotype</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Molecular Chaperones (genetics)</term>
<term>Mutation (genetics)</term>
<term>RNA-Binding Proteins (genetics)</term>
<term>Sarcoglycans (genetics)</term>
<term>Trinucleotide Repeat Expansion (genetics)</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Molecular Chaperones</term>
<term>RNA-Binding Proteins</term>
<term>Sarcoglycans</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Dystonic Disorders</term>
<term>Mutation</term>
<term>Trinucleotide Repeat Expansion</term>
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</keywords>
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<term>Adult</term>
<term>Aged</term>
<term>Female</term>
<term>Genetic Predisposition to Disease</term>
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<front><div type="abstract" xml:lang="en">Task-specific focal upper limb dystonia can be part of the phenotypic spectrum of different types of hereditary dystonia. We investigated whether writer's cramp as presenting symptom is associated with mutations in DYT11, DYT16, or with the DYT1 GAG deletion in 43 patients. No DYT11 and DYT16 mutations were identified. One patient carried the GAG deletion in the DYT1 gene. In our cohort, writer's cramp as presenting symptom is not associated with mutations in DYT11, DYT16, but it can be the sole manifestation of DYT1 GAG deletion mutation carriers.</div>
</front>
</TEI>
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