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Cutis Laxa Panel

Cutis Laxa 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 MyGenome Test

Cutis laxa (CL) is an inherited or acquired connective tissue disorder characterized by wrinkled, redundant, sagging, and inelastic skin associated with developmental and skeletal abnormalities and, in some cases, severe systemic involvement.
The gene mutations underlying Cutis Laxa involve the production of elastic proteins which, forming slender bundles, provide strength and flexibility to the connective tissue. Due to these genetic alterations, the formation, aggregation or functionality of this protein is compromised.
This test is particularly indicated for symptomatic subjects seeking diagnostic confirmation and for family members of an affected subject, in order to evaluate 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:
  • Cutis Laxa
See more about the product

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

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