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Ehlers-Danlos Syndrome Report


Ehlers-Danlos Syndrome Report


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

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

Ehlers-Danlos Syndrome is a group of disorders that affect connective tissues supporting the skin, bones, blood vessels, and many other organs and tissues. Defects in connective tissues cause the signs and symptoms of these conditions, which range from mildly loose joints to life-threatening complications. Correct diagnosis is crucial and must be validated as soon as possible

Along with environmental factors, Genetics plays a key role in the regulation of Ehlers-Danlos Syndrome.


  • 61 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