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9/11/2014 1:47:00 PM | Browse: 793 | Download: 704
Publication Name World Journal of Neurology
Manuscript ID 4234
Country Spain
Received
2013-06-22 13:56
Peer-Review Started
2013-06-22 20:41
To Make the First Decision
2013-08-08 11:28
Return for Revision
2013-08-16 19:45
Revised
2013-09-06 21:29
Second Decision
2013-10-11 14:56
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief
2013-10-12 00:32
Articles in Press
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2013-12-19 18:59
Publish the Manuscript Online
2014-01-16 17:21
ISSN 2218-6212 (online)
Open Access
Copyright
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Neurosciences
Manuscript Type Case Report
Article Title Atypical neurological symptoms associated with CGG expansions of the FMR1 gene
Manuscript Source Invited Manuscript
All Author List Esteban Peña and Marcos Llanero
Funding Agency and Grant Number
Corresponding Author Esteban Peña, MD, Department of Neurology, Hospital Sanitas La Moraleja, Avenida Francisco Pi y Margall no 81, 28050 Madrid, Spain. epenal.pex@sanitas.es
Key Words Fragile X-associated tremor/ataxia syndrome; Fragile X mental retardation; Gray zone; Parkinsonism; Orthostatic tremor
Core Tip In this study we report two atypical cases associated with CGG expansions of the fragile X mental retardation 1 (FMR1) gene. First, a FMR1 premutation alleles carrier presented with a parkinsonism indistinguishable from Parkinson disease. Second, a FMR1 gray zone alleles carrier presented with orthostatic tremor and neurological features associated with the fragile X-associated tremor/ataxia syndrome, such as hand tremor, parkinsonism and ataxia.
Publish Date 2014-01-16 17:21
Citation Pe?a E, Llanero M. Atypical neurological symptoms associated with CGG expansions of the FMR1 gene. World J Neurol 2013; 3(4): 148-151
URL http://www.wjgnet.com/2218-6212/full/v3/i4/148.htm
DOI http://dx.doi.org/10.5316/wjn.v3.i4.148
Full Article (PDF) WJN-3-148.pdf
Full Article (Word) WJN-3-148.doc
Manuscript File 4234-Review.doc
Answering Reviewers 4234-Answering reviewers.pdf
Copyright License Agreement 4234-Copyright assignment.doc
Peer-review Report 4234-Peer review(s).pdf
Scientific Editor Work List 4234-Scientific editor work list.doc