Update on the Clinical, Radiographic, and Neurobehavioral Manifestations in FXTAS and FMR1 Premutation Carriers
Author
dc.contributor.author
Hall, Deborah A.
Author
dc.contributor.author
Robertson, Erin
Author
dc.contributor.author
Shelton, Annie L.
Author
dc.contributor.author
Losh, Molly C.
Author
dc.contributor.author
Mila, Montserrat
Author
dc.contributor.author
Granell Moreno, Esther
Author
dc.contributor.author
Gómez Anson, Beatriz
Author
dc.contributor.author
Martínez Cerdeno, Verónica
Author
dc.contributor.author
Grigsby, Jim
Author
dc.contributor.author
Lozano, Reymundo
Author
dc.contributor.author
Hagerman, Randi
Author
dc.contributor.author
Santa María Vásquez, Lorena Ivette
Author
dc.contributor.author
Berry Kravis, Elizabeth
Author
dc.contributor.author
O'Keefe, Joan A.
Admission date
dc.date.accessioned
2017-03-02T14:14:54Z
Available date
dc.date.available
2017-03-02T14:14:54Z
Publication date
dc.date.issued
2016
Cita de ítem
dc.identifier.citation
Cerebellum. Volumen: 15 Número: 5 Páginas: 578-586 Número especial: SI
es_ES
Identifier
dc.identifier.other
10.1007/s12311-016-0799-4
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/142943
Abstract
dc.description.abstract
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.