Hereditary Myopathies Panel

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

This panel analyzes the main genes responsible for the onset of Hereditary Myopathies, a heterogeneous set of conditions that affect muscle tissue causing weakness and hypotonia. These symptoms may also be associated with histological and structural alterations. The test is therefore useful in the diagnosis of these conditions and inform medical management and support for affected individuals and their families.
Individuals who present signs and symptoms of Hereditary Myopathies typically in childhood or adulthood or for those who have a positive family history for this group of hereditary conditions.

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 150 genes analyzed
  • Investigates SNP and Indel mutations up to 150 bp

List of main conditions:
  • Muscular Dystrophy, Congenital, With Or Without Seizures
  • Muscular Dystrophy-Dystroglycanopathy
  • Nonaka Myopathy

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