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Leber optic atrophy and dystonia

MONDO:0010772

Also known as: Leber optic atrophy and dystonia, LDYT, LHON and dystonia, Leber Hereditary optic neuropathy with dystonia, Leber hereditary optic neuropathy with dystonia, Leber's hereditary optic neuropathy with dystonia, Marsden syndrome, dystonia familial, with visual failure and striatal lucencies

24 clinical trials for this condition and its sub-types.

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Broader categories

Cardiovascular disorder (1051) Disease (680) Heart disorder (300) Metabolic disease (233) Nervous system disorder (231) Musculoskeletal system disorder (207) Hereditary disease (176) Neurodegenerative disease (171) Cardiomyopathy (144) Central nervous system disorder (107)
Trials to join now! 13 Not yet recruiting 1 Not yet finished but already full! 7 Completed 2 Terminated 1
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  • New DNA test could end years of uncertainty for mitochondrial disease patients

    Diagnosis Not yet recruiting

    This pilot study aims to develop a new digital PCR technique to more accurately diagnose mitochondrial diseases. Researchers will test the method on blood, urine, saliva, and muscle fiber samples from 4 patients. If validated, the technique could be faster and cheaper than curren…

    Phase: NA • Sponsor: Centre Hospitalier Universitaire de Nice • Aim: Diagnosis

    Last updated Jun 27, 2026 12:04 UTC

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