Journal article
A qualitative exploration of mothers' and fathers' experiences of having a child with Klinefelter syndrome and the process of reaching this diagnosis
E Bourke, P Snow, A Herlihy, D Amor, S Metcalfe
European Journal of Human Genetics | Published : 2014
Abstract
Klinefelter syndrome (KS) is a common genetic condition that is currently under-diagnosed. The phenotype is broad, with physical, medical and psychosocial features ranging from mild to severe. When a child is diagnosed with KS, the parents may spend months to years searching for a diagnosis. This study used a qualitative methods approach to explore parents' experiences of having a child with KS and receiving a diagnosis. Fifteen semistructured one-to-one in-depth interviews were conducted to explore their experiences and views. The interviews were then transcribed, coded and thematically analysed. The interviews revealed that parents had diverse experiences related to: the timing of the diag..
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Funding Acknowledgements
We acknowledge the parents who participated in this study, without whom this work would not be possible. Also, all individuals at the Murdoch Childrens Research Institute and Monash University who helped bring this study to completion, especially Dr Ned Douglas. This work was supported by the Victorian Government's Operational Infrastructure Support Program.