Cystic Fibrosis Panel

Cystic Fibrosis Panel

Regular price $29.00 USD
Regular price Sale price $29.00 USD
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This product is only meant for customers who already purchased a Dante Genome Test

Cystic fibrosis is a disease that causes thick, sticky mucus to build up in the lungs, digestive tract, and other areas of the body. It is one of the most common chronic lung diseases in children and young adults. It is a life threatening disease.
Mutations underlying Cystic Fibrosis destroy the function of chloride channels, compromising the passage of this ion and of water across cell membranes. As a consequence, the secretion of the exocrine glands will be sticky (with risk of obstruction), while the lungs will produce an excessive amount of mucus.
Test particularly indicated for newborns with suspected diagnosis, for potentially carrier subjects (for example, couples who are planning a pregnancy) and for those who have affected relatives, in order to verify their genetic risk.

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
  • 10 genes analyzed
  • Investigates SNP and Indel mutations up to 150 bp

List of main conditions:
  • Cystic Fibrosis
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This product is only meant for customers who already purchased a Dante Genome Test

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