Wilson Disease Panel
Wilson Disease Panel
Prix habituel
€29.00 EUR
Prix habituel
Prix soldé
€29.00 EUR
Prix unitaire
par
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This product is only meant for customers who already purchased a MyGenome Test
Wilson disease is a rare inherited disorder that causes copper to accumulate in the body, leading to liver damage and neurological symptoms. Wilson disease is caused by mutations in a gene involved in copper transport and metabolism.
This panel is designed for individuals with a family history of Wilson disease or individuals with symptoms of the condition, such as liver disease or neurological symptoms. 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:
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Wilson disease is a rare inherited disorder that causes copper to accumulate in the body, leading to liver damage and neurological symptoms. Wilson disease is caused by mutations in a gene involved in copper transport and metabolism.
This panel is designed for individuals with a family history of Wilson disease or individuals with symptoms of the condition, such as liver disease or neurological symptoms. 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
- 1 or more genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Wilson disease
Ce produit est uniquement destiné aux clients qui ont déjà acheté un test MyGenome.