Cidial Fibrosis: Causes, Symptoms and Treatment

Cystic fibrosis – cf. Under the banner of cystic fibrosis is one of the diseases arising from sticky mucus that looks like a glue, where it accumulates in the body, and leads to the rise of various problems in the internal organs of the body, especially in the lungs and pancreas. People with cystic fibrosis may have trouble breathing and different diseases in the lungs, as well as problems with nutrition, digestion, growth and development. There is no healing for cystic fibrosis, as the symptoms are exacerbated over time, and it is noted that average life (life expectancy) in cystic fibrosis patients has increased over the past forty years as it can reach 30 years, and today there are modern treatments that some patients can reach up to forty years or more. Symptoms of cystic fibrosis are diagnosed with cystic fibrosis, usually at a very early age, and although producing symptoms associated with cystic fibrosis, according to the case, there are very clear symptoms that occur in children with cystic fibrosis, and we mention the following symptoms of the next birth. A lot of salt sweat. diarrhea. Growth disorders, weight gain. Breathing problems. Infection in the lungs. Severe cough. Sficar in the lungs. There are other symptoms that can occur in early childhood, and include the following: hand contracting, where the fingers are round and flat. Recovery, which is the rise of a part of the rectum out of the anus. An enlarged nose or in the sinuses. Causes and factors of the risk of cystic fibrosis are a genetic disease, as both the mother and father should be pregnant with the gene that causes the disease, so that the child is infected. Complications of cystic fibrosis can cause cystic fibrosis many complications on many parts of the body, such as: the digestive system, the respiratory system and the reproductive system. Sicular fibrosis diagnosis shows symptoms of cystic fibrosis in most people with childhood, and tests are performed in the lungs before any symptoms appear. If the results of the tests are positive in the newborn, or in the case of some symptoms that indicate the infection of the cystic fibrosis, the attending physician recommends that the sweat examination be examined to examine the salinity, as people with cystic fibrosis have a high salinity in sweat compared to natural relationships, and that two consistent examination has the diagnosis. The treatment of fallen fibrosis is not a complete treatment for cystic fibrosis, but some available treatments can be used; To improve the quality of the patient’s life. The type of cystic fibrosis treatment varies by the patient, depending on the health problems caused by the disease, and how his body responds to different treatments. Most people get a mix of medical treatment, and some home instructions that can reduce the condition. Prevention of cystic fibrosis is an inaccurate genetic disease, but some issues that prevent the occurrence of complications can be followed cystic fibrosis, such as the following: Be careful to receive all recommended vaccines. Refrain from smoking, or exposure to passive smoking. Use appropriate techniques to clean lung cavities and breathing channels, such as drainage at the time of standing and on the chest. Consume food foods with a high calorie. Medical control regularly undergoes, and make sure you implement the proposed treatment plan by the doctor. In addition, the parents of the newborn, who were diagnosed with cystic fibrosis, are advised to care for the child in the home environment and avoid sending him to a nursery center until he reaches at least six months or a full year.