Phlegm, also known as sputum or mucus, is a substance that can come up during a cough. Phlegm comes from what is known as a productive cough, unlike a dry cough, which does not produce phlegm. Coughing is a normal function, with the purpose of clearing out your airways; however, coughing can also be a symptom of various conditions from allergies to lung disease. Diet can also be a cause or aggravator of coughing and phlegm. Talk to your doctor to determine the cause and treatment options for your phlegm.
You may experience incontinence, bleeding, pain, itching, irritation and protruding red tissue. This condition may stem from chronic constipation and straining during bowel movements, a weak anal sphincter, intestinal parasites...
This mucus buildup causes life-threatening lung infections and serious digestion problems. Omega-3 fatty acids, also known as polyunsaturated fats, and monosaturated fats may help relieve symptoms of cystic fibrosis, as omega-3...
Various medical conditions such as bronchitis or cystic fibrosis may cause mucus to collect in the lungs. Congestion in the lungs may cause symptoms such as coughing and pain in the chest. The symptoms may become bothersome med...
Genetic diseases are caused when a person inherits an abnormal or mutated gene. If an abnormal gene is "dominant," disease develops even if a person inherits the abnormal gene from only one parent and receives a normal gene fro...
According to the Cystic Fibrosis Foundation, cystic fibrosis affects 70,000 people worldwide. It is an inherited disease in which the body produces a thick and sticky mucus due to a gene defect. This mucus can clog the lungs an...
The defective gene causes the body to produce thick mucus that obstructs the lungs and pancreas. Around 66 percent of cases are diagnosed before age 1, but 7 percent present with atypical symptoms and aren't diagnosed until ag...
According to the Cystic Fibrosis Foundation, the median predicted age of survival rose to 37.4 years in 2008, up from 32 years in 2000. The March of Dimes notes that most states routinely screen newborns for CF. Babies with CF...
The Cystic Fibrosis Foundation describes cystic fibrosis, or CF, as an inherited chronic disease. Although CF is invariably fatal, the median predicted age of survival has crept up from age 32 in 2000 to age 37.4 in 2008. The ...
The Mayo Clinic reports that CF happens most often in white people of northern European ancestry, occurring in about one 3,000 live births. Some of the CF symptoms in babies are excessive salty sweat, intestinal blockage and re...
Among children, cystic fibrosis is a common lung disease that may result in early death. Symptoms of cystic fibrosis can vary among children because the gene that causes cystic fibrosis involves more than 1,000 mutations. Howev...
This inherited condition is the result of a gene mutation that causes the body to overproduce mucus. A toddler who develops any of the classic symptoms of cystic fibrosis should receive further evaluation and care from a medica...
Respiratory problems and dietary deficiencies result from this disease. With modern advances in treatment, children born with cystic fibrosis can hope to live into their sixth decade or beyond. Several symptoms typically affect...
Cystic fibrosis (CF), a common genetic disease that causes severe lung disease and other symptoms, has two forms: classic and nonclassic, or atypical. People with the atypical form of cystic fibrosis can have the same symptoms ...
Progressive lung disease, frequent respiratory infections and other complications often place a child with CF in the hospital. Daily treatments with inhaled and oral medications along with other therapies are needed to help rel...
Cystic fibrosis is an inherited, genetic condition common in people of northern European and Ashkenazi Jewish ancestry. People with cystic fibrosis have progressive lung disease that causes frequent infections and trouble clear...
As a child with cystic fibrosis (CF) ages, complications from this chronic disease continue to develop. Respiratory infections can become increasingly hard to treat as different types of bacteria infect the lungs. Teenagers wit...
This disease most commonly affects Caucasian patients during infancy or childhood and, if left untreated, can be fatal. Infants or children who develop signs and symptoms of cystic fibrosis should receive further medical evalua...
According to The Children's Hospital, 30,000 children and adults in the United States are affected by cystic fibrosis. The presence of abnormally thick mucus in the body of a child causes symptoms like meconium ileus.
Cystic fibrosis involves the secretory glands in the body. These glands secrete mucus for lubrication of surfaces within the body. In cystic fibrosis, instead of the mucus being thin, it is thick and tenacious. This leads to cl...
Patients with cystic fibrosis have a gene defect that causes the body to produce excessive amounts of mucus. Approximately 30,000 people in the United States have this condition, according to the Cystic Fibrosis Foundation. The...
One thousand infants are diagnosed with cystic fibrosis every year in America, according to the 2004 report of the Centers for Disease Control and Prevention. Some cystic fibrosis symptoms are seen in newborn babies. Some sympt...
According to the Centers for Disease Control and Prevention, sickle cell anemia is the most common hereditary disease in America that begins in childhood and has no promise of a long life. Cystic fibrosis is number two. As of 2...
The lungs and pancreas are particularly susceptible to the effects of cystic fibrosis. The American Lung Association reports approximately 30,000 Americans are living with cystic fibrosis, which is most often diagnosed in infan...
However, with careful treatment and management of the many complications of the disease, patients are now living several decades: According to the Cystic Fibrosis Foundation, the median age for predicated survival is 37.4 years...
Cystic fibrosis, the most common autosomal recessive inherited disease among Caucasians, was once considered a disease of children, simply because children with the disorder didn't survive to adulthood. In 2010, due to improve...
Cystic fibrosis is a serious, life-threatening disease that can affect the entire body. In most people, digestive fluids, mucus and sweat all are slippery and thin, but with cystic fibrosis this become sticky and thick, the May...
These fluids should be thin and slippery; a defective gene that leads to the development of cystic fibrosis causes them to be thick and sticky, thereby clogging tubes, ducts and passageways. This clogging is particularly danger...
Throughout the 21st century, researchers have been looking into this disease and developing new therapies, and KidsHealth.org says someday there may be a cure. In the meantime, if your child exhibits symptoms, have him diagnose...
Cystic fibrosis is an inherited disease, which means that it is the result of faulty genes being passed from parents to the offspring. Cystic fibrosis is the result of a mutation in a protein that moves chloride (a form of chlo...
This genetic information is passed down through the generations from parents to children. Sometimes parents are only the carrier for the disorder. Some diseases have signs and symptoms as soon as birth, but other disorders may ...
This leads to thick mucus production in those areas. CF is the most common genetic disorder in Caucasians, affecting about 1 in 3,300 infants in the U.S. CF is often diagnosed in infancy, because symptoms begin to affect the ba...
