Authors
Sarah M Coffey, Kylee Cook, Nicole Tartaglia, Flora Tassone, Danh V Nguyen, Ruiqin Pan, Hannah E Bronsky, Jennifer Yuhas, Mariya Borodyanskaya, Jim Grigsby, Melanie Doerflinger, Paul J Hagerman, Randi J Hagerman
Publication date
2008/4/15
Journal
American Journal of Medical Genetics Part A
Volume
146
Issue
8
Pages
1009-1016
Publisher
Wiley Subscription Services, Inc., A Wiley Company
Description
Fragile X‐associated tremor/ataxia syndrome (FXTAS) is generally considered to be uncommon in older female carriers of premutation alleles (55–200 CGG repeats) of the fragile X mental retardation 1 (FMR1) gene; however, neither prevalence, nor the nature of the clinical phenotype, has been well characterized in female carriers. In this study, we evaluated 146 female carriers (mean, 42.3 years; range, 20–75 years) with and without core features of FXTAS (tremor; gait ataxia), and 69 age‐matched controls (mean, 45.8 years; range, 21–78 years). Compared with controls, carriers with definite or probable FXTAS had greater medical co‐morbidity, with increased prevalence of thyroid disease (P = 0.0096), hypertension (P = 0.0020), seizures (P = 0.0077), peripheral neuropathy (P = 0.0040), and fibromyalgia (P = 0.0097), in addition to the typical symptoms of FXTAS–tremor (P < 0.0001) and ataxia (P …
Total citations
2007200820092010201120122013201420152016201720182019202020212022202320242101731224126321843201715141610103
Scholar articles
SM Coffey, K Cook, N Tartaglia, F Tassone, DV Nguyen… - American Journal of Medical Genetics Part A, 2008