Literature DB >> 27017995

Confirmed versus suspected: The social significance of a genetic or non-genetic diagnosis of mitochondrial disease.

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.
Copyright © 2016 Elsevier B.V. and Mitochondria Research Society. All rights reserved.

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


  2 in total

1.  Qualitative exploration of the lived experience of adults diagnosed with primary mitochondrial disease.

Authors:  Kathleen D Valverde; Elizabeth M McCormick; Marni J Falk
Journal:  JIMD Rep       Date:  2022-07-20

2.  Diagnostic odyssey of patients with mitochondrial disease: Results of a survey.

Authors:  Johnston Grier; Michio Hirano; Amel Karaa; Emma Shepard; John L P Thompson
Journal:  Neurol Genet       Date:  2018-03-26
  2 in total

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