what is the role of inj.placentrex in treating submucous fibrosis?how ? and when to be given? whate are the advers effects?
Christine M. Costello has written: 'Investigation of the role of neutrophil proteases and chemotactic agents in the pathogenesis of cystic fibrosis' -- subject(s): Neutrophils, Cyctic fibrosis, Leucocyte elastase
Carriers of cystic fibrosis do not have the disease themselves, as they possess one normal copy and one mutated copy of the CFTR gene. However, they can pass the mutated gene to their children. For a child to develop cystic fibrosis, they must inherit two copies of the mutated gene, one from each parent. Therefore, while carriers do not have cystic fibrosis, they play a crucial role in its inheritance.
The CFTR gene provides instructions for making a protein called the cystic fibrosis transmembrane regulator.
By treating with laughing , with funny activities etc
Adequate protein intake is important for individuals with cystic fibrosis to support growth, development, and maintenance of muscle mass. Protein also plays a role in fighting infection and supporting the immune system, both of which are particularly important in managing the symptoms of cystic fibrosis. However, excessive protein intake is not recommended, as it can put additional strain on the kidneys.
Fibrosis is a pathological process characterized by the excessive accumulation of extracellular matrix components, primarily collagen, leading to scarring and tissue stiffening. While adipocytes (fat cells) can proliferate and play a role in tissue repair, fibrosis specifically refers to the formation of fibrous connective tissue, not the normal division of adipocytes. In some cases, when tissue is damaged, an imbalance between repair and degradation can lead to fibrosis, but this is distinct from the normal regenerative processes involving adipocytes.
Arginine compounds can be used in treating people with liver dysfunction due to its role in promoting liver regeneration.
The lower prevalence of cystic fibrosis in Filipinos is believed to be due to genetic factors. Filipinos may have a different genetic makeup that reduces their risk of developing this condition compared to other populations. Additionally, environmental factors may also play a role in the low incidence of cystic fibrosis in Filipinos.
The role of district public health nurse is to assist in treating community health issues, immunizations, and sexually transmitted disease transmission education.
Someone with non-functional chloride channels may experience cystic fibrosis, a genetic disorder that affects the lungs, digestive system, and other organs. This is because chloride channels play a crucial role in regulating the movement of salt and water in and out of cells, and when they are not functioning properly, it can lead to the production of thick mucus in the body.
It has been discovered that they are also effective in combating some chronic headaches, cancer pain, and pain associated with nerve damage.
Some doctors say that diet plays a role in treating Chron's disease and some doctors say that it doesn't affect it at all. Many people believe that avoiding acidic and high gluten foods helps their digestive system. Many people also use yoghurt to replenish their good gut flora. Eating well is important for general health and medication is important for treating and managing Chron's disease. Getting a proper diagnosis and being treated by a medical professional is imperative.