Cystic fibrosis

In Cystic Fibrosis, symptoms start slowly. The respiratory tract (nose to lungs) and the gastrointestinal (digestive) systems are the most affected. Symptoms usually start in the gastrointestinal system. Male fertility and sweat glands are also affected. Only about fifteen percent of babies who carry the disease have meconium ileus which is sticky and thick caused by thick mucus from intestinal glands. Vomiting and abdominal swelling are caused and surgery right after birth is needed usually. If…

Cystic Fibrosis Cystic fibrosis is a recessive genetic disease in which the lungs and digestive system get filled and clogged up with think sticky mucus. Cystic Fibrosis can also be called Cystic fibrosis of the pancreas, Fibrocystic disease of the pancreas, Mucoviscidosis, Mucoviscidosis of the pancreas, Pancreas fibrocystic disease, Pancreatic cystic fibrosis. This disease affects the cells that control digestive fluids, sweat and mucus in the body, and makes these fluids thicker and…

Genetic Disorder Paper Cystic fibrosis is a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time (cystic fibrosis foundation). It is a decease in the secretory glands, the glands that make mucus and sweat (medicine). It causes the cells in those parts to not function correctly and when needed to produce fluids, produce thick, sticky mucus in the lungs, pancreas and other organs (cystic fibrosis foundation). It builds up and blocks…

Cystic fibrosis SYMPTOMS- there are a couple of major symptoms that include repeated lung infections and the inability to gain weight. Some of symptoms consist of pain areas (in the abdomen), cough ( can be chronic, with blood or with phlegm), gastrointestinal (diarrhoea, heartburn and serve constipation, respiratory (pulmonary hypertension, delayed puberty or slow growth), developmental ( delayed development, delayed puberty or slow growth), whole body ( fatigue or inability to exercise) and…

Cystic Fibrosis is a genetic disorder that prevents how a person’s body make mucus and sweat. It also affects how a person’s lungs and digestive system works. Cystic Fibrosis causes mucus to become very thick, and sweat to be saltier than usual. Thick mucus can make it very hard to breath and can block pancreas, which will make it difficult to digest food properly. Offspring inherits this disease from their parents this illness is common among white people. Doctors can detect Cystic Fibrosis in…

Cystic Fibrosis also known as “CF” is a genetic disorder that can be considered life threatening. This disease is common in the United States and is often found in white newborns. More than 30,000 people in the United States have this disease and approximately 70,000 people worldwide. CF can be screened for in prenatal care visits for early diagnosis. The CF gene was discovered in 1989, research has been supported through the Cystic Fibrosis Foundation. Cystic fibrosis is a progressive genetic…

For many years, researchers have been searching to find a cure for the life-threatening disease, Cystic Fibrosis (CF). Most children are diagnosed around birth from the newborn screening, therefore, this disease takes a toll on the hundreds of children and their families. Families struggle over the stress, emotions and financial problems of caring for children with Cystic Fibrosis. There is still no cure, but patients diagnosed with this dreadful disease are given ways to help proceed with…

Cystic fibrosis (CF) is a life-limiting genetic disorder affecting 70,000 individuals worldwide (about 30,000 in the US). Recent advances in new drug development – approval of Kalydeco and Orkambi - represent a success for the CF community. However, these compounds are not sufficient to cure CF because (a) they show modest improvement in lung function, a key measure for cystic fibrosis patients; (b) efficacy decreases with long term use; and (c) additional drugs are required in patients with…

Cystic Fibrosis is a genetic disorder that occurs mostly in the lungs but is also known to affect the pancreas, kidneys, liver, and intestine (the digestive system). Cystic Fibrosis occurs when neither of a person’s alleles are able to produce the Cystic Fibrosis Transmembrane Conductance Regulator gene, CFTR. This gene is a key component to creating sweat, digestive juices, and mucus in the human body. Cystic Fibrosis has several symptoms, treatments, and impacts on the lives of those who are…

Cystic Fibrosis is an inherited disease of the secretory glands, glands that make up mucus and sweat. It is also known as mucoviscidosis, that affects mostly the lungs but also the pancreas, liver, kidneys and intestine. Long term issues include difficulty breathing and coughing up sputum as a result of frequent lung infections. A defect in the CFTR gene causes cystic fibrosis. This gene makes a protein that controls the movement of salt and water in and out of your body's cells. In people who…