What are the different methods of testing for cystic fibrosis?
cystic fibrosis testing includes genetic screening, newborn screening and sweat testing. The doctor may discuss the possibilities with patients and determine the best choice for the situation. In all cases, if the results are positive, the physician usually recommends following and further testing to confirm the diagnosis and collect further information. This information will be useful for controlling cystic fibrosis of the patient. Cystic fibrosis is a recessive genetic disorder and both parents need a copy of the child to form this condition. Testing for cystic fibrosis can help parents determine whether it is endangered by a child with cystic fibrosis. If only one parent is a carrier, there is no reason to worry. If both carriers are, there is a 25% chance that the child will have a disease.
After children are born, parents can apply for projection of newborns. This is a standard offer in many hospitals. The technician will prick the baby's heel to collect a small sample of blood and send it to the laboratory to projectl Different genetic conditions. Parents should be aware that a positive result in screening of newborns does not mean that a child has a cystic fibrosis. It only means that it can have a disease, and another test is required to diagnose.
The gold standard of cystic fibrosis testing is the sweat test. People with cystic fibrosis produce an unusual amount of sodium chloride in their sweat. In the sweat test, the technique of the chemical applies to the patient to sweat, and uses the electrode to gently stimulate sweat glands and collect the sample. The laboratory analyzes sweat to find out how much sodium chloride is present. Results may be negative, positive or indieterminikae. If the test results are unclear, the patient must repeat the test.
people who are considering cystic fibrosis testing can receive it in most hospitals and clinics. If the device cannot personally test samples, it can send them toLaboratory for analysis and return the result within a few days. Early diagnosis can be decisive for providing interventions that reduce the risk of the patient of future complications. The arrival of testing the newborn on cystic fibrosis in many countries was a significant development in the treatment of cystic fibrosis, because this means that patients can take care of the symptoms.