ABC Medical Center > CYSTIC FIBROSIS MUTATION

CYSTIC FIBROSIS MUTATION

Indications:

No special indications

What it's for:

Confirmation of cystic fibrosis clinical diagnosis. Risk refinement through carrier screening for individuals in the general population. Prenatal diagnosis or familial variant testing when familial variants are included in the 106-variant panel listed in Clinical Information. Risk refinement through carrier screening for people with a family history when family mutations are not available. Identification of patients who may respond to therapy with CFTR enhancers.

Delivery time:

10 business days

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