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Noonan Syndrome Panel

Noonan Syndrome Panel

Prix habituel €29.00 EUR
Prix habituel Prix soldé €29.00 EUR
Vente Épuisé
This product is only meant for customers who already purchased a Dante Genome Test

This panel tests for mutations in genes associated with Noonan syndrome, a genetic disorder that affects many areas of the body. Noonan syndrome is characterized by characteristic facial features, short stature, heart defects, and developmental delays. Testing can help diagnose the condition, identify the genetic cause, and inform medical management and support for affected individuals and their families.
Individuals who have symptoms of Noonan syndrome or a family history of the condition. This may include individuals with characteristic facial features, short stature, heart defects, or developmental delays.

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

List of main conditions:
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Ce produit est uniquement destiné aux clients qui ont déjà acheté un test MyGenome.