{description}As far as genetic diseases go, Cystic Fibrosis is complicated.
Affecting multiple organ systems, Cystic Fibrosis can originate from any combination of over 1000 possible mutations of a single gene. The task of finding a cure for such a disease is understandably daunting, but despite the seemingly bleak outlook, there are many researchers devoted to the case. Cystic Fibrosis, abbreviated CF, is a genetic disorder that causes dysfunction in glands producing mucus, saliva and sweat. As a result, it is commonly manifested along either respiratory or gastrointestinal epithelia. The most common inherited autosomal recessive disease in the United States, its prevalence in the American population has stimulated much laboratory and clinical investigation. Stanford Hospital is home to the largest CF center in California. Clinical studies conducted here often involve large teams of doctors, researchers and both adult and pediatric patients. Without well-orchestrated coordination between these three groups, clinical research might be impossible to conduct. The ability to observe and speak with some of the many different players allows for a unique perspective on CF research at Stanford.{/description}

{description}Finding a cure for a devastating disease{/description}