Sensory Panel
Sensory Panel
Regular price
€29.00 EUR
Regular price
Sale price
€29.00 EUR
Unit price
per
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This product is only meant for customers who already purchased a MyGenome Test
The genetic variants analyzed in this panel are closely related to or potentially the cause of sensory conditions
Sensory panel is a comprehensive panel that tests for genetic variants associated with a wide range of sensory disorders, including hearing loss, vision loss, and neuropathy. These disorders are caused by mutations in genes involved in the development and function of sensory cells and neurons, 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 sensory disorders or individuals with symptoms of these conditions, such as hearing loss, vision loss, and tingling or numbness in the extremities. 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:
Learn More
The genetic variants analyzed in this panel are closely related to or potentially the cause of sensory conditions
Sensory panel is a comprehensive panel that tests for genetic variants associated with a wide range of sensory disorders, including hearing loss, vision loss, and neuropathy. These disorders are caused by mutations in genes involved in the development and function of sensory cells and neurons, 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 sensory disorders or individuals with symptoms of these conditions, such as hearing loss, vision loss, and tingling or numbness in the extremities. 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 15 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Thiourea Tasting
- Developmental Coordination Disorder
This product is only meant for customers who already purchased a MyGenome Test