L0039
LHON (Leber Hereditary Optic Neuropathy): Mitochondrial Diseases
Test Details: Leber Hereditary Optic Neuropathy (LHON), is a maternally inherited disorder resulting in optic nerve degeneration and dysrhythmia. Five mitochondrial point mutations in the gene coding subunits ND1, ND4 and ND6 of NADH-CoQ oxidoreductase have been associated with diagnosis of the disease. Indication for testing are individuals with painless bilateral loss of vision and familial history of the vision related problems in the maternal lineage.
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Category
Molecular Genetics
Pre-test Information
Clinical and family history is mandatory.
Report Delivery
4 working days
Gender
All
Organ
Eyes
LHON (Leber Hereditary Optic Neuropathy): Mitochondrial Diseases
11550
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