Serious long-term consequences, and even fatal complications, can result from deep vein thrombosis, or DVT. In DVT, blood clots form in the deep veins of the body, particularly the lower extremities. These clots can break free, travel to the lung, and block an artery. This circumstance is known as a PE, or pulmonary embolism. Approximately 60,000 to 100,000 deaths occur each year in the United States as a result of DVT associated pulmonary embolism, making it one of the highest causes of unexpected natural death (Andrews & Habashi, 2010).
This leads to foul-smelling, greasy stools, poor weight gain and growth, intestinal blockage, and severe constipation. The average prognosis is about 30 years old. There are several fascinating facts about cystic fibrosis. Nearly 2,500 babies are born with cystic fibrosis in the U.S. each year. More than 10 million Americans carry the cystic fibrosis gene but don’t even know it.
Cystic fibrosis is characterized by the production of abnormal mucus that is excessively thick and sticky. The abnormal mucus leads to blockages within the lungs and airways. This leads to repeated, serious lung infections that can damage the lungs. Lung function often starts to decline in early childhood in people who have cystic fibrosis. Over time, permanent damage to the lungs can cause severe breathing problems.
Myasthenia Gravis Myasthenia Gravis is one of many neuromuscular disorders. It literally means “grave muscle weakness.” This chronic autoimmune neuromuscular disorder affects every “2 per 1,000,000 people per year.” “ The onset is 28 years for female and 42 years for males.” (Aashit K Shah M. , 2011) Muscle weakness occurs and increases with physical activity and usually improves after resting. This muscle weakness is caused by an interruption of the transmission of nerve impulses to the muscles. We can say it’s just the wrong communication to the muscle, preventing voluntary muscles from contracting. Also, “antibodies block receptors for acetylcholine at the neuromuscular junction.” (Aashit K Shah M. , 2011) This neuromuscular junction is a space between nerve endings and muscle fiber.
More than 12 million people are infected in the U.S., while another 12 million people are believed to have the disease but remain undiagnosed. COPD also ranks as the third leading cause of death In the U.S. and is a major cause serious long-term disability. In most cases symptoms of COPD do not appear until substantial lung damage has occurred. People with COPD are also likely to experience
You whole body may also have an affect while dealing with this disease you may feel nauseas or feeling full quicker. Discomfort in the upper abdomen Difficulty falling asleep, chest discomfort, sore throat, Choking sensation and bad breath are also very common symptoms of having
Cystic Fibrosis Research: Cystic Fibrosis (CF) is a complicated genetic disease that causes you to produce extra-thick, sticky mucus. If you or your loved one is fighting this disease, they may require medicines as part of their treatment routine. In the United States, the congenital respiratory disease Cystic Fibrosis (CF) affects about 30,000 children and adults, and 40,000 suffers worldwide according to the cystic fibrosis foundation. About 1000 new cases are diagnosed each year. In 2014, some research, pharmaceutical, and technology breakthrough have helped shed new light on the respiratory disease and continue to inform treatment strategies with the ultimate goal of improving the quality of life for patients and one dying during
People with coronary artery disease build up large amounts of plaque that contains a large amount of cholesterol that builds up inside the coronary arteries. The blood flow to the heart will eventually be impaired, causing damage to the heart muscle. A heart attack is permanent damage, which actually kills a portion of the heart. Sudden cardiac death will occur if the
Cystic fibrosis (CF) Cystic fibrosis (CF), also known as mucoviscidosis, is an autosomal recessive genetic disorder that affects most critically the lungs, and also the pancreas, liver, and intestine. It is characterized by abnormal transport of chloride and sodium across an epithelium, leading to thick, viscous secretions. The name cystic fibrosis refers to the characteristic scarring (fibrosis) and cyst formation within the pancreas, first recognized in the 1930s. Difficulty breathing is the most serious symptom and results from frequent lung infections that are treated with antibiotics and other medications. Other symptoms, including sinus infections, poor growth, and infertility affect other parts of the body.
This gene codes for a protein that form an ion channel, facilitating the movement of salts (sodium and chloride ions) and water across the cell membrane. This is important in creating sweat, digestive juices and mucus [5]. In patients with cystic fibrosis, CFTR is prevented in carrying out these functions due to alteration of salt and water balance in lungs. This eventually causes dehydration in most of the organs and causes thick, sticky mucus to build up in the lungs and digestive tract. Consequently, this creates an environment that favours bacterial growth, and people who suffer from cystic fibrosis are exposed to rapid respiratory tract infections which lead to inflammation and progressive lung