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Congenital Myasthenic Syndrome Report


Congenital Myasthenic Syndrome Report


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


List of genes: