Cystic fibrosis is one of the most frequent genetic diseases in Spain, and in one of our country of births between 5,000 and 7,000 births. Not only that, but one of the 35 Spaniards is estimated to be a healthy carrier of the disease.
According to Dr. Raman Acarro Balbin, a former head of the nemology of the Marcuse de Valtezilla Hospital and a newcomer of the Rodero Center, “Sistic Fibrosis (FQ) is a genetic disorder, a chronic genetic disease, a chronic and kindelous and kindelous and kindelous and kindelous and kindelous and kindelous and kindelous and kindelous. Sweet, drinking water, drinking water, drinking water, drinking water, drinking water, drinking water, drinking water, drinking water, drinking water, drinking water, drinking water, drinking water, drinking water, drinking water, drinking water, drinking, drinking water, drinking water, drinking water, insight, insight, insight, drink, bronchial, drinking, bronchial tubes and sweat.
What is the cause of cystic fibrosis?
When this expert develops, “cystic fibrosis is a mutation in the transmemmprane (CFDR) regulatory gene, which is responsible for the coordination of a particular protein, which is responsible for the coordination of a particular protein.
He also says: “The spread of this disease is the recession of the autosomal, that is, a person should obtain a copy of every parent’s genetic gene, because there is only one congenital copy and another healthy copy of the gene, it will become the carrier of the disease, but it does not create it.”
Symptoms to identify pneumonia
Considering all of this, the symptoms vary mainly depending on the intensity and evolution of the process. According to the affected organs, the symptoms may also be different.
For example, Acarro says that when the respiratory system is affected, the conditional bronchial tubes are prepared by an increase in thick and viscous mucosa, and can be translated into such symptoms:
- Continued cough with a large -thicker mucus expectation
- Infections
- Bronchitis
- Occasionally hematoic expectation
- Respiratory noises (breathing)
- Dyspnea (respiratory difficulty)
- Exercise tolerance
- Nostrils
- Continuous sinusitis
Similarly, in the digestive system, cystic fibrosis (which is the barrier of digestive enzymes from the pancreas to the small intestine, which is a barrier to the absorption of nutrients in the diet):
- Fat feces, obese and bad smell
- Small weight gain and development
- The possibility of a associated diabetic
- Liver problems
- The possibility of intestinal obstruction paintings.
Finally, according to the doctor, other symptoms that may appear:
- Male infertility
- Excessive sweating with excessive salt.
- Astinia, weakness, hypotension (hydro-electrolytic imbalances)
How is it detected
“Detection of cystic fibrosis, is based on the detection of CFDR genetic modifications, and in this sense, this test has created a capital fact that this test has created a capital fact that it has created a capital reality because of the most specific treatment of a very specific treatment.
It continues: “A diagnostic approach is based on the high level of chlorine level in sweat, and then in the respiratory perspective (radiation, sprometry, sputum crops) or digestion (intestinal deception, etc.)” “” “” “” “” “
How is it
The expert recalled that “there is no total treatment for cystic fibrosis,” but emphasizes that “there are an important progress in the quality of life of the patients and the significant reduction in the complications obtained.”
Some of these options are as follows:
- CFDR gene modulators can help improve the functioning of medications and modified protein administered by inhalation.
- Respiratory Physiotherapy with positive techniques for eliminating viscous mucus at the bronchial level.
- Bronchial medications to try to improve bronchial brackets.
- A prediction of specific antibiotic therapy and chronic bronchial infections for persistent infections.
- Food tips with caloric, protein and vitamin supplements.
- Panic enzymes that help food digestion and absorption.
“Thanks to these treatments and the parental genetic council, the life expectancy of the patient and their quality of life have been widely increased in recent years, and in many cases, almost normal life has been created,” Akiro concludes, “Although there is a need for a stable and regular monitoring of medical perspective to evaluate evolution and prevent problems.”
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