The Phenotypic Spectrum of DYT24 Due to ANO3 Mutations
Identifieur interne : 000396 ( Main/Merge ); précédent : 000395; suivant : 000397The Phenotypic Spectrum of DYT24 Due to ANO3 Mutations
Auteurs : Maria Stamelou [Royaume-Uni] ; Gavin Charlesworth [Royaume-Uni] ; Carla Cordivari [Royaume-Uni] ; Susanne A. Schneider [Royaume-Uni, Allemagne] ; Georg K Gi [Royaume-Uni, Suisse] ; Una-Marie Sheerin [Royaume-Uni] ; Ignacio Rubio-Agusti [Royaume-Uni] ; Amit Batla [Royaume-Uni] ; Henry Houlden [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 2014.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Chloride Channels.
- diagnosis : Dystonic Disorders, Myoclonus.
- genetics : Dystonic Disorders, Mutation, Myoclonus.
- Adult, Age of Onset, Aged, Female, Genetic Predisposition to Disease, Humans, Male, Middle Aged, Phenotype.
Abstract
Genes causing primary dystonia are rare. Recently, pathogenic mutations in the anoctamin 3 gene (
Url:
DOI: 10.1002/mds.25802
PubMed: 24442708
PubMed Central: 4150528
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PMC:4150528Le document en format XML
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<author><name sortKey="Bhatia, Kailash P" sort="Bhatia, Kailash P" uniqKey="Bhatia K" first="Kailash P" last="Bhatia">Kailash P. Bhatia</name>
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<term>Dystonic Disorders (diagnosis)</term>
<term>Dystonic Disorders (genetics)</term>
<term>Female</term>
<term>Genetic Predisposition to Disease</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation (genetics)</term>
<term>Myoclonus (diagnosis)</term>
<term>Myoclonus (genetics)</term>
<term>Phenotype</term>
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<term>Myoclonus</term>
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<term>Mutation</term>
<term>Myoclonus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Age of Onset</term>
<term>Aged</term>
<term>Female</term>
<term>Genetic Predisposition to Disease</term>
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<front><div type="abstract" xml:lang="en"><p>Genes causing primary dystonia are rare. Recently, pathogenic mutations in the anoctamin 3 gene (<italic>ANO3</italic>
) have been identified to cause autosomal dominant craniocervical dystonia and have been assigned to the dystonia locus dystonia-24 (DYT24). Here, we expand on the phenotypic spectrum of DYT24 and provide demonstrative videos. Moreover, tremor recordings were performed, and back-averaged electroencephalography, sensory evoked potentials, and C-reflex studies were carried out in two individuals who carried two different mutations in <italic>ANO3</italic>
. Ten patients from three families are described. The age at onset ranged from early childhood to the forties. Cervical dystonia was the most common site of onset followed by laryngeal dystonia. The characteristic feature in all affected individuals was the presence of tremor, which contrasts DYT24 from the typical DYT6 phenotype. Tremor was the sole initial manifestation in some individuals with <italic>ANO3</italic>
mutations, leading to misdiagnosis as essential tremor. Electrophysiology in two patients with two different mutations showed co-contraction of antagonist muscles, confirming dystonia, and a 6-Hz arm tremor at rest, which increased in amplitude during action. In one of the studied patients, clinically superimposed myoclonus was observed. The duration of the myoclonus was in the range of 250 msec at about 3 Hz, which is more consistent with subcortical myoclonus. In summary, <italic>ANO3</italic>
causes a varied phenotype of young-onset or adult-onset craniocervical dystonia with tremor and/or myoclonic jerks. Patients with familial cervical dystonia who also have myoclonus-dystonia as well as patients with prominent tremor and mild dystonia should be tested for <italic>ANO3</italic>
mutations. © 2014 The Authors. Movement Disorders published by International Parkinson and Movement Disorder Society</p>
</div>
</front>
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