Cystic fibrosis CF is an inherited genetic condition found in children that affects the way salt and water move in and out of cells. This, in turn, affects glands that produce mucus, tears, sweat, saliva and digestive juices. Normally, the secretions produced by these glands are thin and slippery, and help protect the body's tissues. In people with cystic fibrosis, the secretions are abnormally thick and sticky, so that they don't move as easily.
Marshall, MD From St.
|Cystic Fibrosis Foundation ~ a very personal connection – Deborah Friedson||It is particularly problematic in the lungs since the mucus accumulates and block the airways, leading to breathing difficulties. Each person inherits two CFTR genes, one from each patient.|
Fink, DSc From St. Stephenson had full access to all of the data in the study and takes responsibility for the integrity of the data, the accuracy of the data analysis, and the decision to submit the manuscript for publication.
The authors acknowledge the support of the U. They also acknowledge and thank all of the patients and families in the United States and Canada who consent to be part of their respective national cystic fibrosis patient registries, as well as the cystic fibrosis clinic staff who spend many hours inputting the data.
Stephenson reports grants from the Cystic Fibrosis Foundation during the conduct of the study and personal fees from Cystic Fibrosis Canada outside the submitted work. Sykes reports grants from the Cystic Fibrosis Foundation during the conduct of the study.
Quon is supported by a Cystic Fibrosis Canada Clinician—Scientist Award, but Cystic Fibrosis Canada played no role in the study design or preparation of the manuscript. Authors not named here have disclosed no conflicts of interest. Disclosures can also be viewed at www. Williams, MD, Deputy Editor, reports that he has no financial relationships or interests to disclose.
Stephenson e-mail, stephensona smh. Requests for Single Reprints: Marshall, Fink, and Elbert; Mr. Analysis and interpretation of the data: Drafting of the article: Critical revision for important intellectual content: Final approval of the article: Administrative, technical, or logistic support: Collection and assembly of data:Cystic fibrosis is a common genetic disease within the white population in the United States.
The disease occurs in 1 in 2, to 3, white newborns. The disease occurs in 1 in 2, to 3, white newborns.
We are a core cystic fibrosis center in Southern California with four affiliate centers located throughout the region. Comprehensive Care Our Center uses a team approach to care for infants, children and adolescents with cystic fibrosis.
Often people with Cystic Fibrosis and families with CF children are not aware of the tax deductions they could make to offset some costs. Watch the videos.
Cystic fibrosis is a serious genetic condition that causes severe damage to the respiratory and digestive systems. This damage often results from a buildup of thick, sticky mucus in the organs. Symptoms of cystic fibrosis can be extremely subtle in children.
Learn about who condition causes, common symptoms, and treatment options. approximately 30, people in the United States have been diagnosed with the condition.
The greatest risk factor for cystic fibrosis is a family history of the disease, especially if either parent is a. According to the Cystic Fibrosis Foundation Patient Registry, in the United States: More than 30, people are living with cystic fibrosis (more than 70, worldwide).
Approximately 1, new cases of CF are diagnosed each year.