Feeding dystonia in McLeod Syndrome
Identifieur interne : 001313 ( Istex/Curation ); précédent : 001312; suivant : 001314Feeding dystonia in McLeod Syndrome
Auteurs : Andreas R. Gantenbein [Suisse] ; Nathalie Damon-Perrière [France] ; Jörg E. Bohlender [Suisse] ; Marie Chauveau [France] ; Chrystelle Latxague [France] ; Marcelo Miranda [Chili] ; Hans H. Jung [Suisse] ; François Tison [France]Source :
- Movement Disorders [ 0885-3185 ] ; 2011-09.
English descriptors
Abstract
Background:: The X‐linked McLeod syndrome belongs to the group of neuroacanthocytosis syndromes and has a Huntington‐disease–like phenotype with a choreatic movement disorder, cognitive alterations, and psychiatric symptoms. Another neuroacanthocytosis syndrome, the autosomal recessive chorea‐acanthocytosis, has a similar presentation, but distinct clinical features, believed to be characteristic, such as tongue protrusion dystonia, feeding dystonia, and rubber‐man–like appearance. Methods:: This work comprised a case series of 3 patients with McLeod syndrome. Results:: The 3 patients with McLeod syndrome developed severe feeding dystonia and tongue protrusion as well as rubber‐man–like appearance in 1 patient during the course of the disease. Conclusion:: These observations indicate that there is an extended phenotypic overlap between McLeod syndrome and chorea‐acanthocytosis. © 2011 Movement Disorder Society
Url:
DOI: 10.1002/mds.23843
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ISTEX:841D3B98EBAC3DC7F05DB4DC94613917A325A591Le document en format XML
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<front><div type="abstract" xml:lang="en">Background:: The X‐linked McLeod syndrome belongs to the group of neuroacanthocytosis syndromes and has a Huntington‐disease–like phenotype with a choreatic movement disorder, cognitive alterations, and psychiatric symptoms. Another neuroacanthocytosis syndrome, the autosomal recessive chorea‐acanthocytosis, has a similar presentation, but distinct clinical features, believed to be characteristic, such as tongue protrusion dystonia, feeding dystonia, and rubber‐man–like appearance. Methods:: This work comprised a case series of 3 patients with McLeod syndrome. Results:: The 3 patients with McLeod syndrome developed severe feeding dystonia and tongue protrusion as well as rubber‐man–like appearance in 1 patient during the course of the disease. Conclusion:: These observations indicate that there is an extended phenotypic overlap between McLeod syndrome and chorea‐acanthocytosis. © 2011 Movement Disorder Society</div>
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