Cystic Fibrosis in infants? - symptoms of cystic fibrosis in infants
My seven month old was sick for 3 months and the restaurant has been reviewed 4 times. She had repeated RSV and wheezing and coughing. The document is now evidence of CF. I am very worried. I'm pretty sure that this not only because he has the symptoms of wheezing, coughing and lung infections. I try to remain calm, but it would if it was devastatd. She had her heel when she was born. Is it only possible to diagnose now. Can anyone offer some advice? Thank you very much.
Sunday, January 10, 2010
Symptoms Of Cystic Fibrosis In Infants Cystic Fibrosis In Infants?
2 comments:
My granddaughter is 14 months and was diagnosed with cystic fibrosis when she 3 weeks ago. It is the most precious child in the world! It is very healthy and has now had several hospital stays. No need to feel devastated, still love your baby and you want to. Make sure that the test is approved by a CF center done. If the diagnosis of cystic fibrosis, it is referred to their local CF center.
madstana --
Cystic fibrosis (CF) is an inherited disease that affects breathing and digestion. Advances in medical treatments have improved the outlook for affected children and adults. However, there is no cure. Some affected people live to the age of 40 years or more.
The abnormal gene that causes CF was discovered in 1989. This discovery led to the development of a test, called the test-makers can help determine which, if a couple is more of a child with cystic fibrosis. The test is routine for couples who have offered a family history of CF. Many providers of health care are also available to test the couples taking account of pregnancy or are pregnant. Couples need to decide whether the evidence is good for them.
What is cystic fibrosis?
CF is an inherited disease that the normal development of salt (sodium chloride) into and out of certain cells, including those affecting the lining of the lungs and the pancreas. This leads to a thick, sticky mucus and other secretions.
The mucus clogs the lungs and cause respiratory irritation. It also offers a reproductionGround for the bacteria to grow. This leads to frequent lung infections, which damage the lungs and contribute to an early death.
Thick gastric juices also clog pipes leading from the pancreas into the small intestine. This prevents fluid from the achievement of the small intestine, where they are needed to digest food. This can lead to digestive problems and slow growth.
How common is CF?
About 30,000 children and adults in the United States has CF. The disease occurs more commonly among Caucasians, but all population groups.
What are the symptoms of cystic fibrosis?
The symptoms of CF are variable and may vary from easy to difficult. Some common symptoms are:
Coughing or wheezing
Lung infections such as pneumonia and bronchitis
Shortness of breath
The slowdown in growth, despite a large appetite
Bowel obstruction called meconium ileus in the newborn (caused by a thickening of the green stool infants usually spend the first days of life)
Greasy, bulky stools
Infertility in men affected by blockagesGE's presence or absence of the tube (vas deferens) sperm from the testicles leads
Many lung infections in patients with cystic fibrosis are caused by a bacterium called Pseudomonas aeruginosa. The bacterium rarely causes problems in people without cystic fibrosis. Antibiotics are often not completely eliminate the bacteria in the lungs. These infections contribute to lung damage.
Most children with CF are well enough to exercise and at school. Doctors recommend exercise for people with CF, because it helps dissolve mucus in the lungs and strengthens the heart and lungs.
How is cystic fibrosis diagnosed?
CF is a sweat test or diagnosis of genetic testing with a sample of blood or saliva. Many children with CF are diagnosed in the first six months of life. About 10 states in all newborn screening for CF, together with other disorders of body chemistry.
About 15 to 20 percent of newborns with CF have meconium ileus. When a baby is this symptom, the physician receives a genetic test to diagnose or rule out CF. Some studies Suggis that to improve early diagnosis and treatment growth of infants and children with cystic fibrosis.
Other children are not diagnosed until they begin to develop other symptoms such as repeated pneumonia or no growth. Children with possible symptoms of CF usually have a sweat test. This simple and painless test measures the amount of salt in sweat. People with CF have more salt in their sweat than healthy individuals. In most cases, is diagnosed with CF at 3 years. Some healthcare providers also recommend a genetic test to confirm the diagnosis.
Both genetic testing and the sweat test is accurate for the diagnosis of cystic fibrosis. However, we can not accurately predict the severity of the symptoms of a child.
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