Cystic Fibrosis Free Essay Example - StudyMoose.
Maria Fotoulaki, Paraskevi Panagopoulou, Eleni Kotsi, and Sanda Nousia-Arvanitakis NUTRITIONAL military position IN cystic FIBROSIS Pediatrics 2008 121: S110If you want to get a full essay, state it on our website: OrderEssay.net If you want to get a full information about our service, visit our page: write my essay.
Cystic Fibrosis Research Paper Essay. Cystic Fibrosis, a very serious inherited genetic disease, is also known as CF and sixty-five roses. This disease affects one in every 3,000 live births. It may first appear in a newborn, but can appear all the way up until a young adult. However, ten percent of most cases are apparent at birth.
Cystic fibrosis is a membrane transport disorder which is commonly affected in the autosomal recessive disease of white populations. It is also identified at birth by a certain condition called ” meconium ileus” which means intestinal obstruction.
Cystic fibrosis causes lung damages from thickened secretions. A risk-related nursing diagnosis for cystic fibrosis would describe interventions that address complications from the disease. For example, recurrent lung infections are a symptom of cystic fibrosis, so “Risk for infection related to chronic pulmonary disease” would be a typical diagnosis.
Cystic fibrosis affects the cells that produce sweat, mucus, and digestive enzymes. Normally, these secreted fluids are thin and smooth like olive oil. They lubricate different organs and tissues, preventing them from getting too dry or infected. In people with cystic fibrosis, however, a defective gene causes the fluids to become wide and sticky.
Among the most common germs causing infections in Cystic Fibrosis patients are Pseudomonas bacteria. This germ is difficult to clear in Cystic Fibrosis patients, even after treatment with antibiotics. Typically, Cystic Fibrosis patients have a pattern of low-grade, persistent infection with periodic worsening, sometimes requiring hospitalization.
Cystic Fibrosis Clinical Medicine and Cellular Pathology Cellular Biochemistry The CFTR (cystic fibrosis transmembrane conductance regulator) gene product is a 168 kD cAMP-regulated chloride channel expressed on epithelial cells in the airways, intestine, reproductive tissues, pancreas, and sweat and salivary glands (Li and Naren, 2005).