Leber hereditary optic neuropathy: utilities and carer burden from British and Irish participants

Leber hereditary optic neuropathy: utilities and carer burden from British and Irish participants

Abstract Background Leber hereditary optic neuropathy (LHON) is a rare, maternally inherited, mitochondrial disease resulting in sudden, progressive central vision loss. The condition affects numerous aspects of daily life, functioning and overall health-related quality of life (HRQL), which may spi...

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Bibliographic Details
Main Authors: Claire Lawrence, Emma Williams, Andrew Mumford, Steve Bojakowski, Julio Benedicto, Andrew Lloyd
Format: Article
Language:English
Published: BMC 2025-05-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Health related quality of life
Utilities
LEBER hereditary optic neuropathy
LHON
Visual acuity
Carer burden
Online Access:https://doi.org/10.1186/s13023-025-03737-w
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