What are the common symptoms of cystic fibrosis?
Cystic fibrosis is a genetic state that affects the body's ability to create secretions such as mucus, digestive juice and sweat. Normally, these substances are neat and highly smooth, allowing them to move easily by body passages. However, in patients suffering from cystic fibrosis, they are dense and sticky and, as a result, accumulate in organs. This can lead to a number of health problems, including breathing, digestive and developmental problems. Although there is no known medicine for this condition, it can learn to recognize common symptoms of cystic fibrosis can be decisive for the commencement of medical intervention and improve the long -term outlook of the suffering. Thus, one of the easiest recognizable symptoms of cystic fibrosis is the noticeably salty taste of the skin of the suffering. Parents often detect this symptom when kissing your child's face.
As a cystic fibrosis, the airways usually cause the airways to connect with a strong viscous mucus, many symptoms of the condition are in the form of respiratory problems. Suffering can experience frequent sinus infectionsand lungs. They may also have chronic breathing problems accompanied by sound reconstruction and constant cough.
Some symptoms of cystic fibrosis are of digestive nature. This is due to the fact that passages that usually carry digestive secretions from the pancreas to the small intestine often often clog in patients with cystic fibrosis, which affects the production and passage of the intestines. As a result, cystic fibrosis often experiences blocking the intestine and constipation. In addition, their bowel movements tend to have a very unpleasant odor and are often greasy or greasy in the constitution.
These digestive problems also tend to prevent the absorption of nutrients consumed food. Proper nutrition is essential for the healthy development of young people. Thus, a common symptom of cystic fibrosis in children is the seeming inability of the child to gain weight accompanied by slow or stopped growth.
While cystic fibrosis is incurable, ofFollowing the understanding of the disease by medical scientists has led to improving treatment methods. With proper treatment, suffering from cystic fibrosis, they can often live until they are 50 years old. This treatment involves antibiotic therapy to avert infections, inhalers to improve breathing, and drugs that decrease respiratory blockages. For maximum efficiency, it is important to start these treatment as soon as possible. Thus, those who detect possible symptoms of cystic fibrosis in themselves or others should consult a doctor immediately.