Test Code 10287
New York approved

Pulmonary Fibrosis and Surfactant Dysfunction Disorders Panel

10 genes

2 - 3 weeks (6 - 12 days STAT)

Who is this test for?
  • Individuals with relevant features who have a clinical or suspected diagnosis of pulmonary fibrosis or surfactant dysfunction disorders 
  • Individuals with features suggesting short telomere syndrome (e.g., premature graying, bone marrow failure)
Method
NGS with CNV (Exome or Genome Platform)
Specimen(s)

Exome Platform: Blood, DNA, Buccal, Saliva, Tissue

Genome Platform: Blood, DNA

Order Options

OTHER OPTIONS
for standard institutional pricing.

Explore related tests

Questions? We can help.

Getting support has never been easier. Let us connect you with our specialists that will assist you with anything from understanding products to navigating insurance questions.

    Prevention Genetics