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Cowden Syndrome Panel

Cowden Syndrome Panel

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

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

Cowden Syndrome is a disorder characterized by multiple noncancerous, tumor-like growths called hamartomas and an increased risk of developing certain cancers. Almost everyone with Cowden syndrome develops hamartomas. These growths are most commonly found on the skin and mucous membranes (such as the lining of the mouth and nose), but they can also occur in the intestine and other parts of the body. The growth of hamartomas on the skin and mucous membranes typically becomes apparent by a person's late twenties.

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

  • 8 genes analyzed
  • 100% genomic regions covered
  • Intragenic and intergenic regions analyzed
  • All variants paneled

List of genes:

AKT1,KLLN,PIK3CA,PTEN,SEC23B,SDHB,SDHC,SDHD


Click here to see all the genes analyzed

Prezzo di listino €49.00 EUR
Prezzo di listino Prezzo scontato €49.00 EUR
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This product is only meant for customers who already purchased a MyGenome Test