Genetic haemochromatosis: A qualitative exploration of patients' experience of diagnosis in primary care
Conference Presentation
Authors | Mortimore, Gerri and Woodward, Amelia |
---|---|
Type | Conference Presentation |
Abstract | Genetic haemochromatosis (GH) is the most common inherited genetic disorder in Caucasians (Bacon et al. 2011), and commonly affects Northern Europeans, especially those with Celtic or Nordic descent, with a ratio of approximately 1:220 - 250 people (Fitzsimmons et al. 2018; Phatak et al., 2008;). Despite the prevalence of GH only 1:5000 people are diagnosed with it (Haemochromatosis UK [HUK] 2019; British Liver Trust [BLT] 2017). |
Keywords | genetic haemochromatosis; GP knowledge; genetic disorder |
Year | 2019 |
Publisher | Royal College of General Practitioner's Annual Primary Care Conference |
Web address (URL) | http://hdl.handle.net/10545/624318 |
hdl:10545/624318 | |
File | File Access Level Open |
File | File Access Level Open |
Publication dates | 24 Oct 2019 |
Publication process dates | |
Deposited | 05 Dec 2019, 11:22 |
Accepted | Sep 2019 |
Contributors | University of Derby |
https://repository.derby.ac.uk/item/94669/genetic-haemochromatosis-a-qualitative-exploration-of-patients-experience-of-diagnosis-in-primary-care
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