Mucoid Pseudomonas aeruginosa
- 8 November 1976
- journal article
- research article
- Published by American Medical Association (AMA)
- Vol. 236 (19), 2190-2192
- https://doi.org/10.1001/jama.1976.03270200028024
Abstract
Two adult patients with cystic fibrosis had late onset of symptoms with principal involvement only of the lungs. The absence of other typical features of cystic fibrosis confused the diagnosis. Recovery of mucoidPseudomonas aeruginosafrom sputum cultures helped to establish the diagnosis in these patients, because these mucoid isolates are rarely obtained from subjects who do not have cystic fibrosis. Recent findings, which have identified the mucoid isolates as predominantly a single strain ofP aeruginosaand have documented its widespread carriage in the United States by patients with cystic fibrosis, point to an interesting epidemiologic relationship between this bacterium and this disease. (JAMA236:2190-2192, 1976)Keywords
This publication has 3 references indexed in Scilit:
- Cystic fibrosis (mucoviscidosis)Published by Taylor & Francis ,2017
- Increasing Incidence of Encapsulated Pseudomonas Aeruginosa StrainsAmerican Journal of Clinical Pathology, 1967
- `Sweat Test' Results in Normal Persons of Different Ages Compared with Families with Fibrocystic Disease of the PancreasArchives of Disease in Childhood, 1960