Yerevan
EN
Lab tests
42-138

Diagnosis of Leber Hereditary Optic Neuropathy (pathogenic variants c.152A>G (p.Tyr51Cys) in the DNAJC30 gene, m.11778G>A, m.14484T>C, m.3243A>G, m.3460G>A, m.8344A>G, m.8993T>G)

Description

Leber Hereditary Optic Neuropathy (LHON) is a rare hereditary mitochondrial pathology affecting predominantly young and middle-aged people, which is characterized by marked painless binocular vision loss and unfavorable prognosis for visual functions. In rare cases, vision may spontaneously recover after several months or years.

Period of execution

Within 10 days. The specified time does not include the day of biomaterial collection

Biomaterial type

  • Venous blood
Total price
51435 ֏
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