Authors
Erving T. Laryea, PhD
Joesph R. Wiencek, PhD, DABCC, FAACC
Department of Pathology, Microbiology, and Immunology
Vanderbilt University Medical Center
Nashville, Tennessee
Primary Audience: Pathologists and Clinical Scientists
Secondary Audience: Residents, Laboratory Technologist/Scientist (Includes all sub-specialty areas), Students, Pathologist Assistants, Laboratory Directors and Educators
Upon completion of this activity, you will be able to:
· identify the CFTR genetic mutation associated with each class of cystic fibrosis;
· recognize the body systems affected by cystic fibrosis and the symptoms associated with them;
· describe the role of laboratory tests in the detection, diagnosis, and confirmation of cystic fibrosis;
· discuss the algorithms followed to diagnose cystic fibrosis; and
· explain how the newer therapy options help in the management of cystic fibrosis.