|
|
||||||||
Guest Access | Sign In via User Name/Password |
|||||||||
1 From the Department of Medicine and Division of Pulmonary and Critical Care Medicine, Washington University School of Medicine and Barnes-Jewish Hospital, St. Louis
Cystic fibrosis (CF) is thought of by most physicians as a disease of children. Advances in therapy have extended the life span of patients so that many pulmonary internists have responsibility for the care of young adults with CF. Nevertheless, the initial diagnosis of CF after the age of 30 years is unusual, and a diagnosis after the age of 60 years is rare. Such a case is reported here.
Key Words: bronchiectasis cystic fibrosis
Submitted on December 17, 1996
Accepted on May 12, 1997
This article has been cited by other articles:
![]() |
M. Gilljam, Y. Moltyaner, G. P. Downey, R. Devlin, P. Durie, A. M. Cantin, J. Zielenski, and D. E. Tullis Airway Inflammation and Infection in Congenital Bilateral Absence of the Vas Deferens Am. J. Respir. Crit. Care Med., January 15, 2004; 169(2): 174 - 179. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. F. Chmiel, M. L. Drumm, M. W. Konstan, T. W. Ferkol, and C. M. Kercsmar Pitfall in the Use of Genotype Analysis as the Sole Diagnostic Criterion for Cystic Fibrosis Pediatrics, April 1, 1999; 103(4): 823 - 826. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |