Genetic counseling for FXTAS and FMR1-associated disorders

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Abstract

Since its identification in 2001, awareness of fragile X-associated tremor/ataxia syndrome (FXTAS) has increased. The number of patients and families impacted by the condition continues to grow. Families with and without a history of fragile X syndrome (FXS) are impacted. Patients are usually identified based on their neurological findings such as intentional tremor, balance and gait difficulties, cognitive impairment, and brain MRI abnormalities.

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Gane, L. W., Howard, K., & Abrams, L. (2010). Genetic counseling for FXTAS and FMR1-associated disorders. In The Fragile X-Associated Tremor Ataxia Syndrome (FXTAS) (pp. 155–176). Springer New York. https://doi.org/10.1007/978-1-4419-5805-1_10

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