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Cowden Syndrome Panel

Cowden Syndrome Panel

Normaler Preis €29.00 EUR
Normaler Preis Verkaufspreis €29.00 EUR
Sale Ausverkauft
This product is only meant for customers who already purchased a MyGenome Test

A rare inherited disorder characterized by the presence of many benign (non-cancerous) growths called hamartomas and an increased risk of cancer. Hamartomas form in different parts of the body, especially the skin, mouth and gastrointestinal tract.
The mutations underlying Cowden Syndrome cause a dysregulation of cell proliferation, which in turn becomes responsible for cancerous growth.
This genetic test is essential to confirm the clinical diagnosis and for those with close relatives affected by the disease.

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

List of main conditions:
  • Cowden Syndrome
Vollständige Details anzeigen

Dieses Produkt ist nur für Kunden gedacht, die bereits einen MyGenome-Test erworben haben.