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Test · Diagnostics

Whole Exome Sequencing +Mitochondrial

Free home sample collection, physician reviewed4 WeeksReports inBloodSample

This test is useful for the genetic analysis when patient presents with mutations in several genes which may have similar clinical presentation eg. neuropathies, ataxia, muscular disorders, skin disorders & thrombocytopenia. It is also useful when phenotype is atypical or combination of symptoms does not provide a definite diagnosis. Mitochondrial mutations linked to various mitochondrial diseases such as Mitochondrial myopathy, MELAS, MERFF, LHON, LEIGH syndrome, Deafness etc.

₹30,000—Members pay ₹29000