Update on the Clinical, Radiographic, and Neurobehavioral Manifestations in FXTAS and FMR1 Premutation Carriers

Fragile X-associated tremor/ataxia syndrome (FXTAS) is a progressive neurodegenerative disorder caused by a repeat expansion in the fragile X mental retardation 1 ( FMR1 ) gene. The disorder is characterized by kinetic tremor and cerebellar ataxia, shows age-dependent penetrance, and occurs more fre...

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Veröffentlicht in:Cerebellum (London, England) England), 2016-10, Vol.15 (5), p.578-586
Hauptverfasser: Hall, Deborah A., Robertson, Erin, Shelton, Annie L., Losh, Molly C., Mila, Montserrat, Moreno, Esther Granell, Gomez-Anson, Beatriz, Martínez-Cerdeño, Verónica, Grigsby, Jim, Lozano, Reymundo, Hagerman, Randi, Maria, Lorena Santa, Berry-Kravis, Elizabeth, O’Keefe, Joan A.
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Sprache:eng
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Zusammenfassung:Fragile X-associated tremor/ataxia syndrome (FXTAS) is a progressive neurodegenerative disorder caused by a repeat expansion in the fragile X mental retardation 1 ( FMR1 ) gene. The disorder is characterized by kinetic tremor and cerebellar ataxia, shows age-dependent penetrance, and occurs more frequently in men. This paper summarizes the key emerging issues in FXTAS as presented at the Second International Conference on the FMR1 Premutation: Basic Mechanisms & Clinical Involvement in 2015. The topics discussed include phenotype-genotype relationships, neurobehavioral function, and updates on FXTAS genetics and imaging.
ISSN:1473-4222
1473-4230
DOI:10.1007/s12311-016-0799-4