Part 2 By the end of Unit 7, you will turn in your completed report and references. Please submit a 5-6 page report (not including reference page),...

Part 2 By the end of Unit 7, you will turn in your completed report and references. Please submit a 5-6 page report (not including reference page), double-spaced, and 12-point font. In your report, please include the following information: 1.Discuss the biochemical or biomedical issue you have chosen 2.Reason for selecting this issue and description of this issue3.Background factors contributing to this issue 4.Local data available 5.Possible problem solving approaches Be sure to include specific examples from the course readings to support your points and to cite in the proper APA style. Cystic fibrosis is an autosomal recessive genetic disorder and it affects the entire body, which in turn leads to progressive disability and even premature death. It was first recognized in 1930. The most serious symptom is difficulty in breathing. There are many other symptoms which include sinus infections, diarrhoea, poor growth and infertility. Cystic Fibrosis is caused because of mutation in the gene accountable for cystic fibrosis transmembrane conductance regulator (CFTR). This gene regulates the components of sweat, mucus and digestive juices. Majorly people without CF have two working copies of the CFTR gene, but only one is needed to avoid cystic fibrosis. CF develops when none of the gene works normally. The vital symptoms of cystic fibrosis are salty tasting skin, inadequate growth and deprived weight gain regardless of a normal food intake; build up of thick, sticky mucus, recurrent chest infections and coughing or shortness of breath. It can also lead to infertility in males because of congenital absence of vas deference in males. Symptoms such as bowel obstruction often become visible during infancy and childhood. Exercise is necessary for the child to release mucus in the alveoli. The inadequate growth in children typically represents inability to gain weight or height and is not detected until investigation is done for poor growth. Cystic fibrosis may also lead to coagulation disorder. NOTE: This is part 2 of my final project. I chose Cystic Fibrosis. Those 2 last paragraphs are my first draght that i submitted to my teacher. You will continue this by answering to the 5 above questions. Please 2 spaces and I need 1 textbook and 1 website sources. Thank you.