Molecular genetic diagnosis of mitochondrial diseases and Leber's optic atrophy (detection of mitochondrial DNA deletions and duplications and 6 common pathogenic variants)

Leber's hereditary optic neuropathy (LHON) is a rare hereditary mitochondrial pathology affecting predominantly young and middle-aged people, characterized by marked painless binocular vision loss and a poor prognosis for visual functions. In rare cases, spontaneous recovery of vision may occur after several months or years.

Within 12 days