Cystic Fibrosis is a genetic disease that seriously affects lungs, liver, intestines and pancreas. Technically speaking, Cystic Fibrosis shortly called as Cf in healing terms is a genetic disorder where the secretory glands in the body are not normal functional. It's a condition which is mostly observed in the childhood of patients, sometimes as early as in their births. Mucus, sweat and other bodily secretions are affected by Cystic Fibrosis and as a ensue they cause serious condition problems for the patients.
Mucus commonly is thin and slippery substance around the lungs which helps to filter, and to dispell dust particles and other micro organisms thus prevents them entering into lungs. For a sick person with that disease, the mucus commonly would be thick and this is what causes breathing problems to the patient. The digestive secretions too are abnormal and don't help food to dispell and vitamins to dispell properly. This is why Cystic Fibrosis affected habitancy are mostly underweight and have a poor increase ratio.
Causes:
The particular main cause of the Cystic Fibrosis is parental inheritance. Like most of the genetic disorders, the Ctfr (Cystic Fibrosis Transmembrane Conductance Regulator), a fault gene will be inherited by the child from their parents who suffer from Cystic Fibrosis. This Ctfr controls the water and salt content in the body cells. So the defected Ctfr gene results in formation thick mucus and releasing excess content of salt in sweat.
Symptoms:
There are far too many symptoms that circulate around the disease thus manufacture it difficult to judge the disease by symptoms alone. And the symptoms too vary from man to man depending upon the disease condition of the patient. Any way there are some basic symptoms of Cystic Fibrosis like symptoms related to respiratory and digestive systems. The first and important symptom is thick mucus around lungs and airways which always causes lung and chest infections.
Chronic cough, pneumonia, abnormal foul smell of bowls, mucus in bowls, improper bowl movements, unusual weight loss, poor growth, abdominal pains, dehydration and excess loss of salt in sweat are the tasteless symptoms of Cystic Fibrosis.
Available Treatments:
At present, there are no major treatments available for Cystic Fibrosis to cure it in a particular sitting or surgery. The approached gene therapy at early stages of disease can bring a convert in defective Ctfr gene. But for the doctor, the most important thing is to minimize the symptoms of disease thus helping sick person to lead a painless life.
The most practiced treatment these days is anti biotic therapy which reduces the disease effects of Cf affected patients and thus addition the average life span of patients drastically. The bronchodilators, mucolytics and decongestants are some of healing practices that ease the breathing theory and sacrifice lung infections in patient.
A specific low fat diet plan can help out solving the digestive problems that plainly come along with the disease. There are also some prescribed exercises and bodily activities that can ease thick mucus and helps to drain quickly. A proper maintenance can help Cf patients to live life normally without many hassles.
To Your Health!
Pancreas Surgery:Cystic Fibrosis - Causes, Symptoms and Treatments
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