Cowden Syndrome Panel
€29.00
/
This product is only meant for customers who already purchased a Dante Genome 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.
List of main conditions:
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
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