Cystic Fibrosis And Pregnancy
Scientists and researchers recently released a study showing a decline in birthrates of babies with cystic fibrosis since genetic testing became available. The general public has more knowledge and understanding of the disease that was a mystery for so long. In medieval times the people believed a baby was “bewitched” when they displayed symptoms of what we now know is cystic fibrosis. With new research and new methods of genetic testing, many hope there will be an another reduction in the birthrate for CF babies. Cystic fibrosis in men will make them sterile, but a woman may still conceive and carry a child to full-term or near full-term.
A child cannot be born with cystic fibrosis unless both of his or her parents are carriers of the mutant gene. That gene was identified in 1988 and is called the cystic fibrosis transmembrane conductance regulator gene. It is associated with the number seven chromosomes. If only one parent is a carrier of the gene, there is a 25 percent chance their child will be a carrier for the disease. There are millions of people in the United States alone who are carriers for cystic fibrosis but do not have signs or symptoms of the disease in their body. Most do not even know they are carriers.
Studies have been conducted on birthrates of children born with cystic fibrosis. A study from Italy shows that babies with cystic fibrosis are often preterm and have a lower than average birth weight. The birth weight was lower than normal for even full-term babies. One of the first signs of cystic fibrosis may be a failure to thrive while eating normally.
Screening for cystic fibrosis in newborns has changed and there are now new ways of testing when the baby is young. The most common form of testing is the sweat test but it is not effective for screening newborn babies. New tests are now being done with the normal blood tests babies have after they are born. The test will be looking for a protein associated with the pancreas and screening their immune system. This would remove the need for a full DNA analysis and can be done at a lower cost.
North America is concentrating on improving quality of life for newborns with cystic fibrosis and finding new ways of treatment. There is no known cure for cystic fibrosis but many new methods of testing, diagnosing, and treating the disease has given CF patients a better quality of life and increased their lifespan.
Your doctor can do genetic testing on you and your partner if there is a history of cystic fibrosis in your family. You may want to consider having the tests done before you decide to get pregnant or add to your family. Testing can be done on babies before they are born to find out if they have cystic fibrosis although there is no way to treat them. The testing gives the parents extra time to learn all they can about the disease and its treatment.
Cystic Fibrosis
The Risk For Being A Carrier For Cystic Fibrosis
Coping Skills After The Diagnosis
Cystic Fibrosis After The Diagnosis
The Spiritual Side Of Cystic Fibrosis Treatment
Drug Treatments Often Prescribed For Cystic Fibrosis
The History Of Cystic Fibrosis
Complications Caused By Cystic Fibrosis
Are You A Carrier Of The Cystic Fibrosis Gene?
Cystic Fibrosis
Introduction To Cystic Fibrosis
... taken for cholera. If a child was diagnosed with cystic fibrosis in the 40's they rarely survived childhood. In the 1970's the survival rate of a child with cystic fibrosis was sixteen! Treatment was supportive in nature and did little more than improve their quality of life. Today there is still no known ...
Preventing Infections In Cystic Fibrosis Patients
... diet can help a patient with cystic fibrosis combat infection. If the disease is affecting the digestive tract a patient can become malnourished because cystic fibrosis affects the pancreas and the enzymes needed to digest your food do not get to the stomach. A higher caloric intake will help with some ...
... why the Cystic Fibrosis gene evolved, they do believe that it may have been because of medicines used to protect earlier generations from cholera. Cystic Fibrosis can be detected by genetic testing before and after the birth of the child. If you have a history of CF in your families, you may want to have ...
Alternative Methods Of Treatment For Cystic Fibrosis
... health and a more positive outlook on life. Physical and psycho activities will help balance your body and relieve stress and tension. You can choose an activity that suits you and within your physical limits. Combining physical exercise with restful meditation can help improve your frame of mind and ...
Genetic Testing And Diagnosis Of Cystic Fibrosis
... normal rate even though they are eating normally should also be taken to a doctor for evaluation. Another test used for newborns is the IRT test. Normally this test is a routine procedure done after the birth of a baby. Blood drawn two or three days after birth is analyzed for a protein called trypsinogen. ...