Leber hereditary optic neuropathy in Slovenia: quality of life and costs from patient perspective

The findings highlight the significant economic and social burden of LHON on patients and their families. Ensuring prompt, accurate diagnosis, access to treatment, financial support, and psychological counselling and services are critical to helping individuals cope with and mitigate the profound challenges of vision loss and living with LHON.

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Institutions

Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2024-08-30
DOI
https://doi.org/10.1186/s13023-024-03329-0
Citations
1
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
0.23

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article

Leber hereditary optic neuropathy in Slovenia: quality of life and costs from patient perspective

Katarína Breciková, M Višňanský, J Zigmond, Lea Kovač et al.
1 citations
Orphanet Journal of Rare Diseases
Mitochondrial Function and Pathology
0.23
article

Leber hereditary optic neuropathy in Slovenia: quality of life and costs from patient perspective

Katarína Breciková, M Višňanský, J Zigmond, Lea Kovač, Aleš Tichopád, Marko Hawlina, Vladimír Rogalewicz, Ivana Šarkanová
article en
1 citations

Abstract

The findings highlight the significant economic and social burden of LHON on patients and their families. Ensuring prompt, accurate diagnosis, access to treatment, financial support, and psychological counselling and services are critical to helping individuals cope with and mitigate the profound challenges of vision loss and living with LHON.

Orphanet Journal of Rare DiseasesVol. 19(1)
Masaryk University (CZ), Ljubljana University Medical Centre (SI), University of Veterinary Medicine in Košice (SK), Valeo (Czechia) (CZ), Czech Technical University in Prague (CZ)
Chiesi Farmaceutici
Decent work and economic growth
Openalex Percentile: Top 43%
Mitochondrial Function and Pathology
0.23
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Leber hereditary optic neuropathy in Slovenia: quality of life and costs from patient perspective — Katarína Breciková, M Višňanský, et al. · Orphanet Journal of Rare Diseases (2024) | TGRS Research Map | TGRS