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Articles Published Processes
9/11/2014 1:47:00 PM | Browse: 858 | Download: 823
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Received |
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2013-06-22 13:56 |
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Peer-Review Started |
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2013-06-22 20:41 |
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To Make the First Decision |
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2013-08-08 11:28 |
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Return for Revision |
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2013-08-16 19:45 |
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Revised |
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2013-09-06 21:29 |
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Second Decision |
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2013-10-11 14:56 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2013-10-12 00:32 |
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Articles in Press |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2013-12-19 18:59 |
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Publish the Manuscript Online |
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2014-01-16 17:21 |
Category |
Neurosciences |
Manuscript Type |
Case Report |
Article Title |
Atypical neurological symptoms associated with CGG expansions of the FMR1 gene
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Manuscript Source |
Invited Manuscript |
All Author List |
Esteban Peña and Marcos Llanero |
Funding Agency and Grant Number |
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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 |
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