Order Cystic Lung Disease Panel (8 Genes) Test
The Cystic Lung Disease Panel sequences 8 genes associated with hereditary lung diseases that are characterized by cystic lung lesions. Hereditary lung diseases identified by variants in these genes include Alpha-1-antitrypsin deficiency disorder, Birt-Hogg-Dubé syndrome, tuberous sclerosis complex-associated lymphangiomeiomatosis (LAM), and cutis laxis and emphysema. Read more about this test.
All samples must be accompanied with a completed requisition form. Please make sure any identifiers used on the specimen is provided on the paperwork. Consent page should be signed by a health care provider. Any incomplete or missing paperwork may delay the start of testing.
EFEMP2, ELN, FBLN5, FLCN, LTBP4, SERPINA1, TSC1, TSC2
- Next Generation Sequencing (copy number analysis included when data meets quality standards)
- Sanger Confirmation
7ml of whole blood (3–5ml for an infant) in a lavender top tube (K2EDTA or K3EDTA)
10 ug of DNA at a minimum concentration of 25 ng/ul (please provide DNA concentration)
The Laboratory for Molecular Medicine offers several billing options for our clients and their patients; however, we do not bill insurance companies and are unable to begin testing without accurate billing information.
81332 (1), 81406 (1), 81407 (1), 81479 (1)
For questions, please contact us at 617-768-8500 or by email.