Physiological Basis of Cystic Fibrosis: A Historical Perspective
- 1 January 1999
- journal article
- review article
- Published by American Physiological Society in Physiological Reviews
- Vol. 79 (1) , S3-S22
- https://doi.org/10.1152/physrev.1999.79.1.s3
Abstract
Quinton, Paul. M. Physiological Basis of Cystic Fibrosis: A Historical Perspective. Physiol. Rev. 79, Suppl.: S3–S22, 1999. — Cystic fibrosis made a relatively late entry into medical physiology, although references to conditions probably reflecting the disease can be traced back well into the Middle Ages. This review begins with the origins of recognition of the symptoms of this genetic disease and proceeds to briefly review the early period of basic research into its cause. It then presents the two apparently distinct faces of cystic fibrosis: 1) as that of a mucus abnormality and 2) as that of defects in electrolyte transport. It considers principal findings of the organ and cell pathophysiology as well as some of the apparent conflicts and enigmas still current in understanding the disease process. It is written from the perspective of the author, whose career spans back to much of the initial endeavors to explain this fatal mutation.Keywords
This publication has 190 references indexed in Scilit:
- Comparison of gastrointestinal pH in cystic fibrosis and healthy subjectsDigestive Diseases and Sciences, 1987
- Environmental deprivation and transient elevation of sweat electrolytesThe Journal of Pediatrics, 1985
- Aminoglycoside clearance inpatients with cystic fibrosisThe Journal of Pediatrics, 1979
- Effect of secretin and graded doses of CCK-PZ on pancreatic secretion in manDigestive Diseases and Sciences, 1974
- Observations on cystic fibrosis of the pancreas. VI. The uterine cervixThe Journal of Pediatrics, 1970
- Quantitative assessment of exocrine pancreatic function in infants and childrenThe Journal of Pediatrics, 1968
- Submaxillary salivary enzymes as a measure of glandular activity in cystic fibrosisThe Journal of Pediatrics, 1964
- Studies of salt excretion in sweat: Relationships between rate, conductivity, and electrolyte composition of sweat from patients with cystic fibrosis and from control subjectsThe Journal of Pediatrics, 1963
- Response of sweat electrolyte concentrations to 9 alpha-fluorohydrocortisone in patients with cystic fibrosis and their familiesThe Journal of Pediatrics, 1963
- Inspissation of secretion, dilatation of the ducts and acini, atrophy and fibrosis of the pancreas in infants: A clinical noteThe Journal of Pediatrics, 1938