Congenital Myasthenic Syndrome Report

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

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

Congenital myasthenic syndrome is a group of conditions characterized by muscle weakness (myasthenia) that worsens with physical exertion.

Along with environmental factors, Genetics plays a key role in the regulation of Congenital Myasthenic Syndrome.

• 29 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