Cystic fibrosis CF can affect all of exocrine (glands secrete fluid into the pipe). Through different pathways leading to abnormal secretion and affect gland function. Some glands, such as the pancreas and small intestine glands, thick secretions or coagulation can be completely blocked glands. Abnormal fluoxetine lung airway mucus gland secretions can clog the airways and cause bacteria. More liquid fluoxetine salt glands, the parotid and salivary secretion containing small.
No meconium ileus in children with cystic fibrosis CF its initial symptoms often after birth weight fluoxetine increase of 4 to 6 weeks of poor, 85% to 90% of patients due to the presence of pancreatic secretion, fat and protein fluoxetine poor digestion and indigestion. Children often have a lot of oily stench of feces and can cause abdominal distension. Even normal appetite or hyperactivity in children is still slow growth, weight loss and muscle relaxation. Fat-soluble vitamins A, absorption D, E and K deficiency can lead to night blindness, fluoxetine rickets, anemia and bleeding disorders. Untreated infants and toddlers, about 20% of the large intestine protruding from the anus in vitro, called fluoxetine rectal prolapse. Dairy products or soy protein-fed infants, because it is not absorbing enough protein and anemia and edema.
Because cystic fibrosis fluoxetine CF can affect most organs, the diagnosis of a variety of other checks also help. Levels decreased as trypsin, fluoxetine digestive enzymes may be prompted to detect fecal trypsin and chymotrypsin levels decreased or lack of increase in fat content. Such as reduced insulin secretion, blood glucose levels will rise. Pulmonary function tests can show respiratory function is impaired. Chest X-ray may also suggest the diagnosis. In addition to the parents of children with cystic fibrosis, their relatives might also want to know whether their children will suffer from the disease. Small blood samples for genetic analysis, you can determine whether the defect in the cystic fibrosis gene. Unless there is at least one such disease genes of the parents, fluoxetine their children will not suffer from cystic fibrosis. If the parents are with this defect in cystic fibrosis gene, each pregnancy, childbirth, their chances of children suffering from cystic fibrosis is 25%. During pregnancy, the fetus for the presence or absence of cystic fibrosis is possible to make an accurate diagnosis.
Differences in the severity of cystic fibrosis CF greatly, depending on the extent of lung involvement, regardless of age. However, disease progression fluoxetine is inevitable, resulting in loss of function, and eventually death. However, in the past 25 years, fluoxetine the prognosis of the disease has been significantly improved, mainly due to today's treatment can delay the onset of certain lung diseases. Half of the patients longer than the lifetime of 28 years. Men, no pancreatic disease, or in patients with initial symptoms confined to the circulatory system, the larger the likelihood of long-term survival. Although there are a variety of diseases, cystic fibrosis patients before death can often be school and work. Gene therapy for the treatment of cystic fibrosis has great prospects.
Each time you eat, inadequate secretion of pancreatic fluoxetine enzyme replacement preparations should be accepted, fluoxetine there is a powder (suitable for children) and capsule formulations to choose from. Food should ensure adequate calories and protein to maintain normal growth and development. The proportion of fat to be normal or high, because patients with cystic fluoxetine fibrosis CF fat malabsorption, they need to consume more fat to ensure proper growth and development. Cystic fibrosis patients should use a double dose of vitamins and water-soluble vitamin E. When exercise, fever or hot weather, patients should fluoxetine add salt. Contains fluoxetine easily digestible protein and fat dairy special, the existence of serious pancreatic diseases in children have some help. Malnourished children, to go through the pipe into the stomach or small intestine complementary foods.
Pneumothorax (Pneumothorax), chronic fluoxetine sinusitis (CPS), chronic pulmonary limitations severe infection, gastrointestinal bleeding, gallbladder disease or bowel obstruction were required surgical treatment. Liver transplantation to treat severe liver damage. Patients with severe heart and lung disease can be the heart and lung transplant. Due to the increase and improvement of methods of experience, so that more common and more successful transplant. One year after transplantation, the survival rate is about 75%, complications improved significantly.
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