Adult cases of congenital muscular torticollis successfully treated with botulinum toxin
Identifieur interne : 001E66 ( Main/Exploration ); précédent : 001E65; suivant : 001E67Adult cases of congenital muscular torticollis successfully treated with botulinum toxin
Auteurs : Manon Bouchard [Canada] ; Sylvain Chouinard [Canada] ; And Oksana Suchowersky [Canada]Source :
- Movement Disorders [ 0885-3185 ] ; 2010-10-30.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Adolescent, Adult, Anti-Dyskinesia Agents (therapeutic use), Bontoxilysin, Botulinum Toxins (therapeutic use), Congenital, Dystonia, Female, Humans, Nervous system diseases, Torticollis, Torticollis (congenital), Torticollis (drug therapy), Treatment, botulinum toxin, cervical dystonia, congenital muscular torticollis, torticollis, treatment.
- MESH :
- chemical , therapeutic use : Anti-Dyskinesia Agents, Botulinum Toxins.
- congenital : Torticollis.
- drug therapy : Torticollis.
- Adolescent, Adult, Female, Humans.
Abstract
Congenital muscular torticollis (CMT) is the most common cause of torticollis in childhood. This condition is usually recognized and successfully treated in infancy, but may persist in adulthood, particularly if not treated. In adult patients, CMT can be differentiated from idiopathic cervical dystonia by the frequent association with facial asymmetry, presence of a cord‐like sternocleiodmastoid muscle (SCM), absence of head tremor, lack of sensory trick, and head tilt since infancy. We describe 3 patients with persistent CMT, who were successfully treated with botulinum toxin injections with long lasting benefit. © 2010 Movement Disorder Society.
Url:
DOI: 10.1002/mds.23371
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Congenital muscular torticollis (CMT) is the most common cause of torticollis in childhood. This condition is usually recognized and successfully treated in infancy, but may persist in adulthood, particularly if not treated. In adult patients, CMT can be differentiated from idiopathic cervical dystonia by the frequent association with facial asymmetry, presence of a cord‐like sternocleiodmastoid muscle (SCM), absence of head tremor, lack of sensory trick, and head tilt since infancy. We describe 3 patients with persistent CMT, who were successfully treated with botulinum toxin injections with long lasting benefit. © 2010 Movement Disorder Society.</div>
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