Cystic Fibrosis - Cystic Fibrosis Symptom, picture, Causes, Treatment
Cystic Fibrosis is an
illness which impacts the secretion of
degrees of severity. The most
of cystic fibrosis (CF)
production of thick, sticky mucus in the lungs and pancreas, and
secretion of salt by the sweat and salivary glands.
about 1 in 2500 children. It develops when a child
a recessive gene for CF from every parent. The parents are not
impacted, but have a 1 in 4
of having an
child. In Australia the blood of most new-born babies is
checked to see whether they are
Other than CF is
descry soon : after birth due to the signs of steatorrhoea or of bowel obstruction by thick, sticky meconium (the contents of the baby's intestine) such as vomiting, and a
Symptom of Cystic Fibrosis
The symptoms and austerity of CF
from person to person. Several people with CF have
lung and digestive dilemmas. Other people have
disease which doesn't show up until they are adolescents or young adults.
Signs and symptoms in children and young adults
The signs and symptoms of cystic fibrosis in children and
adults may include:
to the skin. People with cystic fibrosis
to have higher than usual amounts of salt (sodium chloride) in their sweat. This may be one of the first signs parents
the salt when they kiss their child.
- Barricade in the bowels.
- Detain growth.
- Thick sputum. It's
for parents to
this sign because young children tend to swallow their sputum rather than cough it up.
- Coughing or wheezing.
- Common chest and sinus infections with
pneumonia or bronchitis.
- Protuberance of part of the rectum by the anus (rectal prolapse). This is
induced by stools which are
to pass or by frequent coughing.
- Extension or rounding (clubbing) of the fingertips and toes. Although clubbing
in most people with cystic fibrosis, it also appears in several people
with heart disease and
types of lung
Cystic fibrosis also may be
- Evolvement, (polyps) in the nasal passages
- Cirrhosis of the liver due to
of the bile ducts
- Rearrangement of one part of the intestine into
part of the intestine (intussusception) in children older than age 4
Treatment of Fibrosis
Cystic fibrosis (CF) is an
disease of your mucus and
your lungs, pancreas, liver, intestines, sinuses, and sex organs. Teatment includes digestive enzymes taken as tablets or powder, antibiotics for chest infections,
physiotherapy, and the
of a mist tent to loosen mucus in the air passages.
for most patients is
to drain mucus from your child's lungs. Your
or respiratory therapist can
you the best manner to perform this lifesaving approach.
Most CF sufferers
to die in childhood, but with progress in treatment over the last 40 years, many now
to adulthood. Treatments for cystic fibrosis are intention at
symptoms and complications.