Cystic Fibrosis Background

September 11, 2020

A person who has only one CF gene is. It causes respiratory and digestive problems because.

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A child will be born with CF only if they inherit one CF gene from each parent.

Cystic fibrosis background. Cystic fibrosis CF is a genetic condition that affects a protein in the body. Through a defective gene in cells that produce mucus digestive fluids and sweat the normally low-viscosity liquids are not produced as such. Background Cystic fibrosis Cystic fibrosis is an inherited disease that causes thick sticky mucus to build up in the lungs and digestive tract.

At this time people thought a salty child was bewitched Gray pg18 Then during the 1900s doctors began to suspect it to be a symptom of an unknown disease. Tracking Down the Origins of Cystic Fibrosis in Ancient Europe CF is the most common genetic disease among Caucasians and how it became so widespread is something of a mystery. In people with CF mutations in the cystic fibrosis transmembrane conductance regulator CFTR gene cause the CFTR protein to become dysfunctional.

Dorothy Andersen provided the first description of the disorder in the medical literature calling the disease cystic fibrosis of the pancreas based on her autopsy findings of children who died of malnutrition. Cystic fibrosis is an inherited disease characterized by the buildup of thick sticky mucus that can damage many of the bodys organs. The disorders most common signs and symptoms include progressive damage to the respiratory system and chronic digestive system problems.

This means that it is inherited. The disease is characterized by abnormal functioning of exocrine glands. As such the digestion of fats proteins and carbohydrates becomes ineffective.

Cystic fibrosis is a progressive genetic disease that causes persistent lung infections and limits the ability to breathe over time. Cystic fibrosis CF is a genetic disease. Background information on Cystic Fibrosis CF Cystic Fibrosis is a genetic disorder caused by mutations of the cystic fibrosis transmembrane conductance regulator CFTR gene.

Cystic Fibrosis has a long past dating back to the 1700s. People who have cystic fibrosis have a faulty protein that affects the bodys cells tissues and the glands that make mucus and sweat. The symptoms materialize because the condition impairs the digestive system.

In 1938 American pathologist Dr. Both internal mucus and external secretions sweat produced by exocrine glands are altered in patients with this condition. Cystic fibrosis CF is the most common genetically inherited condition in European-derived populations.

However it is being increasingly recognised in other populations including people of Asian Black African and Caribbean descent. We will write a custom Essay on Cystic Fibrosis. Background Cystic Fibrosis is an inherited disorder that severely damages the lungs and digestive systems of the individuals in which it is found.

It affects approximately 30000-35000 people in the United States. It is the most common type of chronic lung disease in children and young adults and may result in early death. Mucus is normally slippery and protects the linings of the airways digestive tract and other organs and tissues.

Diagnosis and Patient Background specifically for you for only 1605 11page. Background on Cystic Fibrosis and COVID19 The Cystic Fibrosis Foundation is a national organization actively engaged in the research and development of new therapies for cystic fibrosis a rare lifethreatening genetic disease that affects more than 30000 people in the United States. Cystic fibrosis CF is a genetic disease.

Cystic Fibrosis Cf Young Men S Health