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 chlorine) throughout the...
Vitamin K is a fat soluble vitamins. Deficiency from low dietary intake is rare but possible. Some populations are susceptible to vitamin K deficiency, however. If the body is running low, symptoms such as bleeding gums and hematuria, or blood in...
People who have the genetic disease called cystic fibrosis (CF) have a problem with the enzymes that are produced in the pancreas. The pancreas is a small gland in the body which secrets enzymes that, through a network of ducts, flow into the...
Whether itâs tofu or soy milk, there are certain components that soy foods have in common. Called isoflavones, theyâre a unique class of phytochemicals (disease-fighting plant compounds). Isoflavones actually function as a weak form of...
Lungs are protected by a thin film of fluid that surrounds them. People with cystic fibrosis (CF) have a gene mutation that causes sticky mucus. This mucus surrounds lung and other internal organs. CF patients also have an issue with salt...
The pancreas is an organ, located in the abdomen, which produces and secretes several hormones and digestive enzymes, including an enzyme called lipase that is necessary to break down fats to free fatty acids. A disease called cystic fibrosis...
A cell mutation is an accidental change in the genetic code, or DNA. Most mutations cause a protein to be missing or malformed. Some genetic mutations are inherited, while others occur as a result of environmental factors, such as UV radiation,...
Genes are the individual building blocks that provide information for how the body is built. When a gene is damaged or mutated, information may be lost, and the result may be a genetic disease. An analogous situation would be baking from a recipe...
Cystic fibrosis is a chronic disease that affects more than 30,000 infants, toddlers, children and adults throughout the United States, according to the Cystic Fibrosis Foundation. This inherited condition is the result of a gene mutation that...
Genetic mutations cause permanent changes in a DNA sequence that makes up a gene, according to Medline Plus. Mutations can range in size, varying from a single DNA block to a large segment of a chromosome. Individuals inherit genetic mutations...
Turmeric has been used both in food and in medicine for over 4,000 years. It has a unique flavor and a bright yellow color which easily stains. It comes from the root of the Curcuma longa plant. Fresh turmeric powder can be made by boiling,...
The lungs are made up of a number of tissue types that facilitate inspiration, the transfer of oxygen and carbon dioxide between the air and the bloodstream, and expiration of carbon dioxide. Lungs connect to the windpipe, or trachea, by a number...
Several lung diseases may be caused by protein-related problems. According to the University of Maryland Medical Center, there are numerous types of lung problems that require the attention of a physician or other qualified health care...
According to MedlinePlus, a service of the National Library of Medicine and the National Institutes of Health, cystic fibrosis is an inherited disease that causes thick, sticky mucus to build up in the lungs and digestive tract. Among children,...
Your child's teeth may come in yellow or green for a variety of reasons. Yellowish teeth may or may not be cause for concern, but green teeth will need attention from your dentist. Antibiotic use, health conditions and exposure to metals can all...
Genetic diseases are passed down from parent to child through defective genes. Genes, the basic unit of heredity, carry the sequences of deoxyribose nucleic acid (DNA) which is responsible for determining the characteristics a person will exhibit....
Cystic fibrosis, or CF, is an inherited disease, which occurs most commonly in the Caucasian population. According to the Mayo Clinic, CF occurs in about 1 out of every 3000 live births. The disease develops when a baby inherits two copies of a...
Genetic diseases occur because of abnormal genes or chromosomes. Causes of genetic diseases include mutated genes, chromosome duplication, missing chromosomes and a portion of a chromosome erroneously attaching to another chromosome. Some genetic...
The human genome--the whole of a person's DNA--contains thousands of genes. Each person has two copies of most genes, called alleles, with one allele inherited from the mother and one from the father. During development and throughout life, the...
