Von Willebrand Panel
€29.00
/
This product is only meant for customers who already purchased a Dante Genome Test
Von Willebrand disease (VWD) is a blood disorder in which the blood doesn't clot properly. Blood contains many proteins that help blood clot when needed. One such protein is called von Willebrand factor (VWF).
Von Willebrand is a bleeding disorder caused by a deficiency or dysfunction of von Willebrand factor, a protein involved in blood clotting. Von Willebrand disease is caused by mutations in the von Willebrand factor gene, and this panel tests for genetic variants that are known to affect these processes.
This panel is designed for individuals with a family history of bleeding disorders or individuals with symptoms of the condition, such as easy bruising, nosebleeds, and heavy menstrual bleeding. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
List of main conditions:
Von Willebrand disease (VWD) is a blood disorder in which the blood doesn't clot properly. Blood contains many proteins that help blood clot when needed. One such protein is called von Willebrand factor (VWF).
Von Willebrand is a bleeding disorder caused by a deficiency or dysfunction of von Willebrand factor, a protein involved in blood clotting. Von Willebrand disease is caused by mutations in the von Willebrand factor gene, and this panel tests for genetic variants that are known to affect these processes.
This panel is designed for individuals with a family history of bleeding disorders or individuals with symptoms of the condition, such as easy bruising, nosebleeds, and heavy menstrual bleeding. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members.
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 5 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Von Willebrand
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