Alport Syndrome Panel

This product is only meant for customers who already purchased a Dante Genome Test

Alport Syndrome panel is used to identify genetic variants associated with Alport syndrome, a rare inherited disorder that affects the kidneys and can lead to hearing loss and vision problems. This panel tests for genetic variants in genes that encode collagen, a protein that is important for the structure and function of the kidneys, inner ear, and eyes.
This panel is designed for individuals with a family history of Alport syndrome or for those who have symptoms of the condition, such as blood in the urine, proteinuria, hearing loss, and vision problems. Early diagnosis through genetic testing can help inform treatment and management decisions, including kidney function monitoring, hearing and vision assessments, and supportive care. It 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 8 genes analyzed
  • Investigates SNP and Indel mutations up to 150 bp

List of main conditions:
  • Alport Syndrome

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