Date of Award

1999

Document Type

Thesis

Department

Philosophy

First Reader

Dr. Isaac Mwase

Second Reader

Dr. Joe Jeffers

Third Reader

Dr. Randall Wight

Abstract

Cystic fibrosis (CF) is a progressive, multisystem disease whose etiology is a genetic mutation in the CF gene product, cystic fibrosis transmembrane conductance regulator (CFTR). The disorder affects all exocrine glands, with common symptoms involving the lungs and pancreas. Although the CF gene and its protein product have been identified, two aspects of the disease make CF particularly difficult to diagnose and manage: (a) variability in both degree and pattern of the mutation in different individuals and (b) lack of information regarding the precise molecular and cellular mechanisms responsible. Let us begin by examining the pathogenesis and pathophysiology of the disease and current diagnosis, treatment, and research in gene therapy.

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