Cystic fibrosis definition

Cystic fibrosis means a multisystem genetic disorder in which defective chloride transport across membranes causes dehydration of secretions. The result is a production of a thick, viscous mucus that clogs the lungs. This leads to chronic lung infections, fatal lung disease, and also interferes with digestion. Early detection and treatment can prevent malnutrition, and enhance surveillance and treatment of lung infections.

Cystic fibrosis means a life-shortening disease caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR), a transmem- brane protein involved in ion transport. Affected individuals suffer from chronic, progressive pulmonary disease and nutritional deficits. Early detection and enrollment in a com- prehensive care system provides improved outcomes and avoids the significant nutritional and growth deficits that are evident when diagnosed later.

Cystic fibrosis means a congenital disorder caused by defective functioning of a transmembrane regulator protein and charac- terized by damage to and dysfunction of various organs, such as the lungs, pancreas, and reproductive organs.

Examples of Cystic fibrosis in a sentence

• Examples of Prescription Drugs that are considered Specialty Pharmaceuticals include some orally administered anti-cancer Prescription Drugs and those used to treat the following conditions: Crohn’sDisease; Infertility; Hemophilia; Growth Hormone Deficiency; RSV; Cystic Fibrosis; Multiple Sclerosis; Hepatitis C; Rheumatoid Arthritis; and Gaucher’s Disease.

• Examples of Prescription Drugs that are considered Specialty Pharmaceuticals include some orally administered anti-cancer Prescription Drugs and those used to treat the following conditions: Crohn’s Disease; Infertility; Hemophilia; Growth Hormone Deficiency; RSV; Cystic Fibrosis; Multiple Sclerosis; Hepatitis C; Rheumatoid Arthritis; and Gaucher’s Disease.

• Suggested data availability language: Data are available upon request through the Cystic Fibrosis Foundation Patient Registry/ Comparative Effectiveness Research Committee.

• It is the policy of the Cystic Fibrosis Foundation to protect patient information from unauthorized access or use at all times, and to assure that this information will only be utilized, transferred, and/or stored in sanctioned and approved ways to provide the strictest confidentiality of the patients in our national Patient Registry database.

• Cystic Fibrosis Foundation Patient Registry Data Application and Confidentiality Agreement All data requests must be submitted as described below, noting: • For all members of the project team: Name, title, address, phone, e-mail, role on the project, and whether they need access to CF Foundation Patient Registry data.

More Definitions of Cystic fibrosis

Cystic fibrosis means an inherited, life-threatening disorder that affects the cells that produce mucus, sweat and digestive juices that causes severe damage to the lungs and digestive system. The Diagnosis must be based on a sweat test with results of chloride concentrations greater than 60 mmol/L.

Cystic fibrosis means the definite Diagnosis of a genetic disease affecting the sweat and mucous glands particularly in the lungs and digestive system, characterized by excess production of thick mucous leading to chronic progressive respiratory disease and nutritional problems.

Cystic fibrosis means a congenital disorder caused by defective functioning of a transmembrane regulator pro- tein and characterized by damage to and dysfunction of various organs, such as the lungs, pancreas, and reproduc- tive organs.

Cystic fibrosis means any one or all of the human diseases commonly known as cystic fibrosis.

Cystic fibrosis means an inherited disorder of the exocrine or outward secreting glands of the body, causing those glands to produce abnormally thick secretions of mucus.

Cystic fibrosis. (also known as CF or mucoviscidosis) means a hereditary disease caused by a mutation in a gene called the cystic fibrosis transmembrane conductance regulator (CFTR), which governs the production of certain bodily secretions (sweat, digestive juices, mucus). The condition is characterized by lung disease, which results from clogging of the airways due to mucosa build-up and leads to recurring cycles of infection and inflammation and difficulty in breathing, which often results in progressive lung failure and death in relatively young individuals.

Cystic fibrosis means a life-shortening disorder caused by mutations in the gene encoding the cystic fibrosis transmembrane con- ductance regulator (CFTR), a transmembrane protein involved in ion transport. Affected individuals suffer from chronic, progressive pul- monary disease and nutritional deficits. Early detection and enroll- ment in a comprehensive care system provides improved outcomes and avoids the significant nutritional and growth deficits that are evi- dent when diagnosed later.