Feeding dystonia in McLeod Syndrome
✍ Scribed by Andreas R. Gantenbein; Nathalie Damon-Perrière; Jörg E. Bohlender; Marie Chauveau; Chrystelle Latxague; Marcelo Miranda; Hans H. Jung; François Tison
- Book ID
- 102504217
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 366 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
✦ Synopsis
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
📜 SIMILAR VOLUMES
Mancozeb is a ethylene-bis-dithiocarbamate (EBDC) fungicide that contains zinc and manganese. 1 In humans, chronic EBDC inhalation has been associated with neurocognitive impairment and parkinsonism 2 while acute intoxication elicit reversible headache, dizziness, and seizures in a few cases, all of
## Abstract The X‐linked McLeod neuroacanthocytosis syndrome strongly resembles Huntington's disease and has been reported in various countries world‐wide. Herein, we report two Chilean brothers with predominant psychiatric features at disease onset including schizophrenia‐like psychosis and obsess
## Abstract Myoclonus–dystonia syndrome (MDS) is an autosomal dominant disorder characterized by bilateral myoclonic jerks. An 8‐year‐old boy presenting with early onset, medically intractable, MDS due to a mutation in the ϵ‐sarcoglycan gene (SGCE) underwent chronic bilateral stimulation of the glo