[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address Please contact the publisher to request reinstatement.
[Skip to Content Landing]
September 1994

Diagnosis of Cystic Fibrosis in a Premature Infant via Neonatal Screening-Reply

Author Affiliations

Department of Pediatrics University of Wisconsin—Madison 600 Highland Ave Madison, WI 53792-4108

Arch Pediatr Adolesc Med. 1994;148(9):996. doi:10.1001/archpedi.1994.02170090109030

This article is only available in the PDF format. Download the PDF to view the article, as well as its associated figures and tables.


The case described by Allen and colleagues is a good example of the value of molecular testing in the diagnosis of cystic fibrosis in a premature infant. Cystic fibrosis should always be high on the list of diagnoses in an infant who is failing to thrive despite adequate energy intake, and molecular testing can be very helpful when sweat testing is not feasible.

None of these observations constitute an argument for routine, involuntary, population screening of all newborns or premature infants. Decisions about population screening must include much more complex considerations, including psychological and medical benefits and risks, costs, and respect for ethical and legal traditions of informed consent.

First Page Preview View Large
First page PDF preview
First page PDF preview