This product is only meant for customers who already purchased a MyGenome Test

CMT is a rare hereditary neuropathy affecting the peripheral nervous system, particularly the lower extremities. This disease can lead to different outcomes, from insignificant variations in motor skills to limb atrophy, with a series of related effects such as difficulty walking and muscle pain.

The genes involved are many and each is responsible for a different form of the disease.

This test is useful for subjects for whom the diagnosis of CMT arises, in order to identify the gene involved, but also for asymptomatic subjects with a family history of the disease, in order to evaluate the risk of onset.

The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.

• Available in less than 24 hours
• Based on Whole Genome Sequencing
• More than 70 genes analyzed
• Investigates SNP and Indel mutations up to 150 bp

Click here to read the full list of the genes analyzed in this panel