M0090
Mitochondrial Mutation Panel-2
Number of Tests | 6 |
Test Included | LHON, NARP, CPEO, SNHL, DEAF, AMDF |
Test Details: Mitochondrial diseases are a clinically heterogenous group of disorders that arise as a result of dysfunction of the mitochondrial respiratory chain. Epidemiological studies have shown that mitochondrial disorders affect at least one in 8000 of the general population. The MITOMAP database has confirmed the association of the mitochondrial mutations with the pathogenesis of mitochondrial disorders.
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Category
Molecular Genetics
Pre-test Information
Clinical and family history is mandatory.
Report Delivery
6 working days
Gender
All
Organ
Multi-Organ
Mitochondrial Mutation Panel-2
14685
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