Autosomal dominant optic atrophy and peripheral neuropathy

MONDO:0016646

Autosomal dominant optic atrophy and peripheral neuropathy (ADOAPN) is a form of autosomal dominant optic atrophy (ADOA), characterized by progressive and isolated visual loss in the first decade of life, decreased reflexes in the lower limbs and a mild cerebellar stance.

17 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant optic atrophy and peripheral neuropathy itself.

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↑ Mitochondrial oxidative phosphorylation disorder (58) ↑ Autosomal dominant optic atrophy (6)

Including sub-types (17) Tagged with Autosomal dominant optic atrophy and peripheral neuropathy (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.