| Literature DB >> 27017995 |
Elizabeth Krieg1, Laurel Calderwood2, MaryAnn Campion2, Katherine E Krepkovich2.
Abstract
This study assessed attitudes and beliefs regarding the importance of a genetic versus non-genetic diagnosis within the mitochondrial disease community. Survey respondents were categorized into two groups - those with a genetic diagnosis, and those with a non-genetic diagnosis of mitochondrial disease. We found that while both groups perceive problems with the support available to adult mitochondrial disease patients, the non-genetic group experiences less medical and social support due to lack of a definitive diagnosis. Understanding the efficacy of existing resources for mitochondrial disease sub-groups will allow for the development or improvement of resources designed to meet patient needs.Entities:
Keywords: Adult patient population; Diagnosis; Genetic testing; Mitochondrial disease; Patient experience; Physician education
Mesh:
Year: 2016 PMID: 27017995 DOI: 10.1016/j.mito.2016.03.008
Source DB: PubMed Journal: Mitochondrion ISSN: 1567-7249 Impact factor: 4.160