Unfortunately, there is none at this time. Sucks for me.
If by vector you mean the organism which causes it, there is none. Cystic fibrosis is a genetic condition.
why are Enzymes are used as pharmaceutical supplements to treat cystic fibrosis disorder
cystic fibrosis
cystic fibrosis
A lavender-top tube, also known as an EDTA tube, is commonly used to draw blood for cystic fibrosis testing. This tube is used for collecting whole blood samples for analysis, such as genetic testing for cystic fibrosis.
A medical physician can run a test known as the chloride sweat test that can be used to help diagnose cystic fibrosis. Cystic Fibrosis is a systemic disease that primarily affects the lungs and causes thick mucous secretions to build up in the airway and therefore causes breathing problems.
Cystic fibrosis is often associated with the color teal, which symbolizes awareness for the disease. This color is used in campaigns and events to promote understanding and support for those affected by cystic fibrosis. Teal ribbons are commonly seen during awareness months and events dedicated to the condition.
Good Question. The answer is cystic fibrosis is not contagious, however, people with cystic fibrosis tend to carry bacterial infections that can cause serious issues to other people with CF, so infection control procedures should be used when two or more cystics are around each other. General population folks need not fear of getting cystic fibrosis from others - it's a hereditary disease.
a nebulizer is an item that is used for some cystic fibrosis paitece.
Perhaps cystic fibrosis?Cystic Fibrosis-- Final answer. CFTR channels malfunction and Chloride cannot exchange with bicarb at the epithelial surfaces exposed to the environment. Chloride then gets stuck outside the environment.
Gene therapy for cystic fibrosis involves delivering a functional copy of the CFTR gene to affected cells in order to restore normal function of the protein. This can be achieved by using viral vectors to deliver the gene into the cells and allow it to produce normal CFTR protein. By correcting the underlying genetic defect, gene therapy holds promise for treating cystic fibrosis at the molecular level.