Friedreich ataxia - what we have learned in 160 years

Friedreichova ataxie (FA) pedstavuje nejastj autozomln recesivn ddinou ataxii. Jej patogenetickou podstatou je mitochondriln dysfunkce v dsledku snen exprese genu FXN pro protein frataxin. Prvn pznaky FA se objevuj charakteristicky ve druh dekd ivota ve vku mezi 10 a 15 lety. I pes kontinuln intenzivn vzkum zstv zatm FA nevylitelnou nemoc. Omaveloxolon pat do specifick tdy liv nazvanch modultory Nrf2 (nuklern transkripn faktor) a je prvnm lkem schvlenm pro pacienty s FA, jen zasahuje pmo do patofyziologie nemoci. Omaveloxolon pin pacientm nadji na zpomalen progrese onemocnn a vznamn zlepen kvality ivota.

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Publication Details

Journal
Neurologie pro praxi
Published
2024-09-10
DOI
https://doi.org/10.36290/neu.2024.046
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
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article

Friedreich ataxia - what we have learned in 160 years

Simona Halúsková, Martin Vališ, Pavlína Hemerková, David Matyáš
Neurologie pro praxi
Genetic Neurodegenerative Diseases
article

Friedreich ataxia - what we have learned in 160 years

Simona Halúsková, Martin Vališ, Pavlína Hemerková, David Matyáš
article en

Abstract

Friedreichova ataxie (FA) pedstavuje nejastj autozomln recesivn ddinou ataxii. Jej patogenetickou podstatou je mitochondriln dysfunkce v dsledku snen exprese genu FXN pro protein frataxin. Prvn pznaky FA se objevuj charakteristicky ve druh dekd ivota ve vku mezi 10 a 15 lety. I pes kontinuln intenzivn vzkum zstv zatm FA nevylitelnou nemoc. Omaveloxolon pat do specifick tdy liv nazvanch modultory Nrf2 (nuklern transkripn faktor) a je prvnm lkem schvlenm pro pacienty s FA, jen zasahuje pmo do patofyziologie nemoci. Omaveloxolon pin pacientm nadji na zpomalen progrese onemocnn a vznamn zlepen kvality ivota.

Neurologie pro praxiVol. 25(4)
Openalex Percentile: Top 84%
Genetic Neurodegenerative Diseases
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