Mitochondrial disease: a challenge for the caregiver, the family, and society

J Child Neurol. 2013 May;28(5):663-7. doi: 10.1177/0883073813481622. Epub 2013 Mar 25.

Abstract

Mitochondrial diseases represent a genetically and clinically heterogeneous group of inherited metabolic disorders, often resulting in poor functional and survival outcomes for the patient and considerable psychosocial distress for the caregiver. The systematic review undertaken in the present paper emphasizes the critical role of the caregiver in the management of a child with mitochondrial disease, with focus on the burden of mitochondrial disease on the caregiver, the family, and society.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Activities of Daily Living / classification*
  • Activities of Daily Living / psychology*
  • Anxiety Disorders / diagnosis
  • Anxiety Disorders / genetics
  • Anxiety Disorders / psychology
  • Caregivers / psychology*
  • Child
  • Cost of Illness*
  • Depressive Disorder / diagnosis
  • Depressive Disorder / genetics
  • Depressive Disorder / psychology
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Male
  • Mitochondrial Diseases / genetics
  • Mitochondrial Diseases / psychology*
  • Mitochondrial Diseases / therapy*
  • Mothers / psychology
  • Personality Inventory
  • Quality of Life / psychology*
  • Social Support*
  • Stress, Psychological / complications