Full metadata
Title
Cystic Fibrosis
CF
Description
Cystic fibrosis (CF) is a fatal, inherited disease found in humans and characterized by buildup of thick, sticky mucus, particularly in the respiratory and digestive tracts. The abnormally thick mucus prevents the pancreas from functioning normally; it often leads to digestive problems and chronic lung infections. Cystic fibrosis is most prevalent in Caucasian individuals, and approximately 1 in every 29 individuals in the US is a carrier for the mutated CF gene. There are an estimated 30,000 reported cystic fibrosis cases in the US, and 70,000 reported cases worldwide, although the international number is undoubtedly low due to underreporting or early deaths.
Date Created
2012-01-01
Contributors
Topical Subject
Keywords
- Concept
- Disorders
Language
eng
Primary Member of
Peer-reviewed
Yes
Open Access
Yes
Handle
https://hdl.handle.net/10776/1965
System Created
- 2023-01-25 08:59:39
System Modified
- 2023-04-20 05:31:32
- 1 year 6 months ago
Additional Formats