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Cystic Fibrosis: A Deadly Disease Affecting 30,000 Children 
 
by Valencia P. Higuera September 07, 2005

Symptoms of Cystic Fibrosis

The symptoms of cystic fibrosis vary. Those who have CF are born with the condition. In most cases, physicians will be able to detect signs of cystic fibrosis within days of birth. However, there have been cases when children were not diagnosed with the condition until their teenage years. They likely exhibited mild symptoms during their early years that did not trigger red flags. Symptoms of cystic fibrosis include:

  • Blockage of small intestines: Babies born with CF generally do not have a bowel movement within the first 48 hours of life
  • Salty tasting skin
  • Recurrent respiratory problems
  • Weight loss during infancy
  • Slow growth rate
  • Wheezing
  • Chronic cough
  • Failure to gain weight after birth
  • Poor appetite

Initially, parents may not perceive the signs of cystic fibrosis. Babies develop differently. They are also exposed to bacteria that may cause numerous infections. However, during routine check-ups, pediatricians are generally able to identify any abnormalities that point to CF. Moreover, parents should report any signs of cystic fibrosis to their infant's doctor. Additional signs include a sudden worsening of cough or wheezing, sudden onset of breathing difficulties, and foul-smelling stools. Parents who suspect CF should not automatically conclude the worse. Cystic fibrosis is a rare illness, and only affects approximately 3,000 newborns a year. The root of symptoms could be one of many less serious, treatable conditions. Nonetheless, ignoring mild symptoms may cause more harm to a baby's health.

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