Charcot-Marie-Tooth Disease Report

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

The Charcot-Marie-Tooth Disease Report is based on Whole Genome Sequencing Test. As such, it analyzes all Common and Rare Variants associated with Charcot-Marie-Tooth Disease instead of a limited set of genes, like old genetic target panels.

Charcot-Marie-Tooth disease encompasses a group of disorders known as hereditary sensory and motor neuropathies that damage the peripheral nerves. Damage to the peripheral nerves that worsen over time may result in alteration or loss of sensation and wasting (atrophy) of muscles in the feet, legs, and hands. 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.

Along with environmental factors, Genetics plays a key role in the regulation of Charcot-Marie-Tooth Disease.

• 78 genes analyzed
• 100% genomic regions covered
• Intragenic and intergenic regions analyzed
• All variants reported
  
  
  

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