Free Delivery Over $100
|
|
|||
|
||||
OverviewCystic fibrosis (CF) is an inherited existence-threatening ailment that affects many organs. It reasons adjustments inside the electrolyte transport gadget inflicting cells to soak up an excessive amount of sodium and water. CF is characterized via troubles with the glands that make sweat and mucus. Symptoms begin in early life. On common, humans with CF live into their mid to past due 30. Cystic fibrosis (CF) is a genetic disorder, this means that you get if from your dad and mom at beginning. It affects the way your body makes mucus, a substance that helps your organs and systems paintings. Mucus ought to be skinny and slippery, however when you have CF, it turns into thick and glue-like. This blocks tubes and ducts throughout your frame. Through the years, this thick mucus builds up inside your airways. This makes it tough to respire. The mucus traps germs and leads to infections. It is able to additionally purpose excessive lung harm like cysts (fluid-crammed sacs) and fibrosis (scar tissue). That's how CF were given its call. More than 30,000 human beings inside the U.S. Stay with cystic fibrosis. Medical doctors diagnose approximately 1,000 new cases each yr. Full Product DetailsAuthor: Dr D V DanielsPublisher: Independently Published Imprint: Independently Published Dimensions: Width: 14.00cm , Height: 0.20cm , Length: 21.60cm Weight: 0.050kg ISBN: 9798851299315Pages: 32 Publication Date: 06 July 2023 Audience: General/trade , General Format: Paperback Publisher's Status: Active Availability: Temporarily unavailable  The supplier advises that this item is temporarily unavailable. It will be ordered for you and placed on backorder. Once it does come back in stock, we will ship it out to you. Table of ContentsReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |
||||
