Cystic Fibrosis (CF) is a very common, potentially life threatening condition. The disease is caused by inheritance, and affects the exocrine glands of the patient. Cystic fibrosis is found primarily among Caucasians and those of European descent. Those diagnosed with Cystic Fibrosis battle daily to perform simple tasks, such as breathing, as the mucus in their bodies thickens immensely. This mucus will potentially accumulate in the patient’s vital organs, such as the lungs, pancreas, and intestines. One can determine if he/she has cystic fibrosis by analyzing certain symptoms. Cystic Fibrosis can be diagnosed according to the symptoms the patient shows, and can be treated through specific types of treatments, such as gene therapy.
Cystic Fibrosis is a lifelong disease that has a harsh negative affect on many vital organs, some of which include the lungs, pancreas, and intestines. This disease causes the mucus, tears, and sweat of the patient to be considerably thick. However, the thickness of such mucus is determined by the severity of the patient’s Cystic Fibrosis. This mucus affects the breathing of those diagnosed with cystic fibrosis, and many have reported an additional trouble with digesting food. One is most likely to have Cystic Fibrosis if their families have a history of such a disease. Therefore, Cystic Fibrosis is a genetic disease that is recessively passed down to proceeding generations. Additionally, this disease most commonly affects those who are Caucasian or of European descent.
Those who have relatives diagnosed with Cystic Fibrosis are at an automatic increased risk to have the disease. For example, in order for a child to have cystic fibrosis, their parents must be carriers of the CF gene. “One CF gene from each parent will result in a pregnancy with a : - One-in-four chance a child will have CF - Two-in-four chance a child will not have CF – but will carry the CF gene - One-in-four chance each baby will NOT have CF and NOT be a CF carrier (How Do Parents Pass on the CF Gene).” Unfortunately, many are unaware that the gene is carried in their families. Because of this, one should always be cautious if showing the symptoms of Cystic Fibrosis.
Cystic Fibrosis is a very common genetic disease. Unbeknownst to them, one in twenty-five people have this genetic disorder. Therefore, one should always be on the lookout for signs of Cystic Fibrosis. A major symptom of this disease includes clubbing of the fingers, which results in the inflammation of the patient’s fingers or toes. Patients may also experience coughing and wheezing, abdominal pain, infertility (in men), weakness and fatigue, and unintentional weight loss. It is recommended that if one experiences any of these symptoms, they immediately contact their doctor or physician. However, doctor may not be able to diagnose a patient strictly from their symptoms, so further genetic testing may be necessary.
Genetic testing may be needed in order to accurately determine...