M0098
MM (Mitochondrial Myopathy) - Mitochondrial Disease
Test Details: Mitochondrial myopathy is a neuromuscular disorder, associated with three mutations in the mitochondrial tRNA encoding genes of Leu(A3302G), Ser(G7497A) and Glu(T14709C). The age of onset and the clinical course of diseases caused by mitochondrial mutations are highly variable. The heteroplasmy also underlies the phenotypic variability, characteristics of mitochondrial diseases.
Category
High End
Pre-test Information
Clinical and family history is mandatory.
Report Delivery
4 working days, Test Schedule: Mon-Sat, Cutoff: 14:00 hrs
Gender
All
Organ
Multi-Organ
MM (Mitochondrial Myopathy) - Mitochondrial Disease
6050
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