{"id":407679,"date":"2025-09-19T00:30:00","date_gmt":"2025-09-18T22:30:00","guid":{"rendered":"https:\/\/medizinonline.com\/neuroimaging-biomarkers-in-friedreichs-ataxia\/"},"modified":"2025-09-19T02:00:15","modified_gmt":"2025-09-19T00:00:15","slug":"neuroimaging-biomarkers-in-friedreichs-ataxia","status":"publish","type":"post","link":"https:\/\/medizinonline.com\/en\/neuroimaging-biomarkers-in-friedreichs-ataxia\/","title":{"rendered":"Neuroimaging biomarkers in Friedreich’s ataxia"},"content":{"rendered":"\n

Friedreich’s ataxia<\/strong> (FA) is a rare, autosomal recessive neurodegenerative disease whose natural history and clinical characterization have made significant progress in recent decades. Nevertheless, there is still a lack of sensitive, objective biomarkers that both reliably reflect disease progression and are practicable for clinical studies. The TRACK-FA study, the largest multicenter, multimodal neuroimaging study in FA to date, is now making a decisive contribution. It shows that structural and functional imaging markers not only detect disease-relevant changes, but also correlate with clinical scales. This opens up new avenues for more precise diagnostics, the development of therapies and the shortening of study durations. <\/strong><\/p>\n\n

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Friedreich’s ataxia (FA) is a rare, autosomal recessive neurodegenerative disease whose natural history and clinical characterization have made significant progress in recent decades. Nevertheless, there is still a lack of……... <\/p>\n

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