Cystic fibrosis affects
the secretory glands
, which make mucus and sweat because it disrupts the normal function of epithelial cells – cells that make up the sweat glands in the skin and that also line passageways inside the lungs, liver, pancreas, and digestive and reproductive systems.
What part of the human body cell is affected by cystic fibrosis?
Cystic fibrosis is a condition which mainly affects
the lungs and pancreas
but can affect other parts of the body, including the liver, nose and sinuses and sweat glands. Normally, cells in these parts of the body make mucus and other watery juices and secretions.
How does cystic fibrosis affect the cells?
Cystic fibrosis affects the cells that
produce mucus, sweat and digestive juices
. These secreted fluids are normally thin and slippery. But in people with CF , a defective gene causes the secretions to become sticky and thick.
What organelle does cystic fibrosis affect?
In most kids with cystic fibrosis, says Balch, the CFTR protein gets stuck inside the cells in a cell organelle known as
the endoplasmic reticulum
—a convoluted membranous sac within the cell where the synthesis of proteins like CFTR and other vital cell functions take place.
What cell type is affected by cystic fibrosis?
We conclude that, of the three cell types in secretory coil, only
the beta-S cell
is specifically affected in the CF secretory tissue of the human sweat gland.
What gender is cystic fibrosis most common in?
Males
account for slightly more than 50 percent of all cases of cystic fibrosis (CF) but generally have better outcomes than females until about age 20.
Can you have cystic fibrosis without lung problems?
But new research suggests that this pulmonary view of cystic fibrosis is only half of the picture: a suite of symptoms associated with cystic fibrosis can also
occur in patients who do not have lung disease at all
, indicating that cystic fibrosis is really two diseases.
What is the life expectancy for cystic fibrosis?
Many young adults with CF finish college or find jobs. Lung disease eventually worsens to the point where the person is disabled. Today, the average life span for people with CF who live to adulthood is
about 44 years
. Death is most often caused by lung complications.
What are the physical effects of cystic fibrosis?
CF
causes thick mucus that clogs certain organs
, such as the lungs, pancreas, and intestines. This may cause malnutrition, poor growth, frequent respiratory infections, breathing problems, and chronic lung disease.
What don’t we know about cystic fibrosis?
Cystic fibrosis is
an uncommon genetic disorder
. It primarily affects the respiratory and digestive systems. Symptoms often include chronic cough, lung infections, and shortness of breath. Children with cystic fibrosis may also have trouble gaining weight and growing.
How is cystic fibrosis caused?
Cystic fibrosis is an
inherited disease caused by mutations in a gene called the cystic fibrosis transmembrane conductance regulator (CFTR) gene
. The CFTR gene provides instructions for the CFTR protein.
What type of condition is cystic fibrosis?
Cystic fibrosis is
a progressive, genetic disease that causes persistent lung infections
and limits the ability to breathe over time. In people with CF, mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene cause the CFTR protein to become dysfunctional.
How can cystic fibrosis be diagnosed?
A complete diagnostic evaluation for CF should include a
sweat chloride test, a genetic or carrier test
, and a clinical evaluation at a CF Foundation-accredited care center. Most children are now screened for CF at birth through newborn screening and the majority are diagnosed by age 2.
Is CF curable?
There’s no cure for cystic fibrosis
, but a range of treatments can help control the symptoms, prevent or reduce complications, and make the condition easier to live with. Regular appointments to monitor the condition are needed and a care plan will be set up based on the person’s needs.
Can you live a long life with cystic fibrosis?
While there is no cure yet for cystic fibrosis (CF),
people with CF are living longer
, healthier lives than ever before. In fact, babies born with CF today are expected to live into their mid-40s and beyond. Life expectancy has improved so dramatically that there are now more adults with cystic fibrosis than children.
Can you get cystic fibrosis at any age?
While cystic fibrosis is
usually diagnosed in childhood
, adults with no symptoms (or mild symptoms) during their youth can still be found to have the disease.
