Congenital Myasthenic Syndrome ReportRegular price €49.00 EUR
Please note that these reports are recommended only for Whole Genome Test with 30X and up coverage
(Not compatible with WGL Longreads 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.
Click here to see what your report will look like
- 29 genes analyzed
- 100% genomic regions covered
- Intragenic and intergenic regions analyzed
- All variants reported
List of genes: