Order Bronchiectasis Panel (17 Genes) Test
The Bronchiectasis Panel sequences 17 genes associated with hereditary lung diseases that cause localized, irreversible dilation of the bronchi, and obstructive lung disease. Hereditary lung diseases identified by variants in these genes include cystic fibrosis and primary ciliary dyskinesia. Read more details 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.
CCDC39, CCDC40, CFTR, DNAAF1, DNAAF2, DNAH11, DNAH5, DNAI1, DNAI2, DNAL1, NME8, RSPH1, RSPH4A, RSPH9, SCNN1A, SCNN1B, SCNN1G
- 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.
81223 (1), 81406 (3), 81479 (1)
For questions, please contact us at 617-768-8500 or by email.