Journal article
“Both Sides of the Wheelchair”: The Views of Individuals with, and Parents of Individuals with Friedreich Ataxia Regarding Pre-symptomatic Testing of Minors
GC Lowe, LA Corben, RE Duncan, G Yoon, MB Delatycki
Journal of Genetic Counseling | Published : 2015
Abstract
Friedreich ataxia (FRDA) is an autosomal recessive neurodegenerative disorder characterized by variable age of onset, with no treatment proven to alter its natural history. Siblings of individuals with FRDA have a 25 % risk of developing the condition, raising issues around genetic testing of asymptomatic minors. There is a lack of professional consensus and limited empirical evidence to support provision or refusal of testing. This study aimed to ascertain the opinions of individuals with and parents of individuals with FRDA regarding pre-symptomatic testing of minors. A qualitative research approach using semi-structured interviews and thematic analysis was employed. Interviews with ten in..
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Funding Acknowledgements
The authors thank all participants who generously took the time to participate. RED was partly supported through The Invergowrie Foundation. LAC is an Early Career Fellow of the National Health and Medical Research Council (Australia). This study was supported by the Victorian Government's Operational Infrastructure Support Program.