Keep them breathing: Cystic fibrosis pathophysiology, diagnosis, and treatment
Sheena D Brown1, Rachel White, Phil Tobin
1Sheena D. Brown is a clinical assistant professor at Mercer University in Atlanta, Ga. Rachel White practices at Precision Bone and Joint in Austin, Tex. Phil Tobin is director and an associate professor in the PA program at Touro University Nevada. The authors have disclosed no potential conflicts of interest, financial or otherwise.
Abstract:
Cystic fibrosis (CF) affects more than 30,000 people in the United States and 80,000 people worldwide. This life-threatening genetic disorder causes a buildup of thick, viscous mucus secretions in various organ systems, most commonly the gastrointestinal, pulmonary, and genitourinary systems. This article reviews the clinical manifestations, diagnosis, and monitoring of patients with CF as well as guidelines for management and emerging pharmacologic treatments.
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