Describe in detail the pathophysiological process of cystic fibrosis

Describe in detail the pathophysiological process of cystic fibrosis
SAMPLE APPROACHES
Complications in cystic fibrosis patients differ depending on the extent of transmutation of the cystic fibrosis transmembrane conductance regulator (CFTR) (Brown, White, & Tobin, 2017). CF is defined by atypical excudations that cause blockages in the pulmonary, gastrointestinal, and reproductive tracts (Brown, White, & Tobin, 2017). According to the literature, there may be additional CF-linked primary defects, such as an intrinsic proinflammatory condition and abnormal immune protection in the lungs (Brown, White, & Tobin, 2017). CF is caused by a transmutation caused by a defect in the CF transmembrane conductance regulator gene. The CFTR polypeptide is a cyclic adenosine monophosphate (cAMP)-activated chloride medium that exists on the surface of many different types of epithelial cells, including those lining the trachea, bile ducts, pancreas, sweat glands, and vas deferens (McCance, Huether, Brashers, & Rote, 2013). Despite the fact that CF is a multiorgan medical condition, lung pathosis is the cause of patients’ sudden death. This causes airway surface liquid depletion in the lung, which leads to ciliary collapse and reduced mucociliary transport because airway surface liquid is important for ciliary balance and function (Brown, White, & Tobin, 2017). As a result, a vicious circle of mucus retention occurs, resulting in pestilence of the small airways and chronic inflammation (Brown, White, & Tobin, 2017).
OR
CF is associated with deficient epithelial chloride ion transport (McCance et al., 2013). The CF gene can be found on chromosome 7
Describe in detail the pathophysiological process of cystic fibrosis
and has six classifications that differ in severity (McCance et al., 2013). Research states that “the cystic fibrosis transmembrane conductance regulator (CFTR or CFTR) gene mutation results in the abnormal expression of cystic fibrosis transmembrane conductance regulator protein, which is a cyclic adenosine monophosphate (cAMP)-activated chloride channel present on the surface of many types of epithelial cells including those lining the airways, bile ducts, the pancreas, sweat ducts, and the vas deferens” (McCance et al., 2013).
Most commonly the CF genetic mistake is the DF508 protein that results in hypochloremia that progresses to lung issues related to thick mucus which inhibits proper air exchange that leads to infections, lung damage, and could ultimately lead to respiratory failure (CFF, n.d.). Patients display a variety of symptoms from the salty-tasting skin, to a cough, frequent respiratory infections, wheezing, dyspnea, clubbing, poor weight gain even though there is a good appetite, and stools can range from greasy to difficulty in having bowel movements (CFF, n.d.). The patient is five months old (the median age at diagnosis is six months), is experiencing greasy, foul-smelling diarrhea, small for her age, coughing, and wheezing, which are classic symptoms of CF. If the disease presents itself later in life, the patients typically have milder symptoms as opposed to diagnosing the patient within the first year of life. The severity of the disease depends on which class it falls in; classes 4-6 experience milder symptoms than those that fall within classes 1-3 (McCance et al., 2013). CF must be diagnosed early to improve the patient’s quality and longevity of life. After recognizing the symptoms, one must confirm their differential before giving a definite diagnosis. Screening newborns for CF is a universal protocol in the United States.

Struggling to find relevant content or pressed for time? – Don’t worry, we have a team of professionals to help you on
Describe in detail the pathophysiological process of cystic fibrosis
Get a 15% Discount on this Paper
Order Now
Calculate the price
Make an order in advance and get the best price
Pages (550 words)
$0.00
*Price with a welcome 15% discount applied.
Pro tip: If you want to save more money and pay the lowest price, you need to set a more extended deadline.
We know how difficult it is to be a student these days. That's why our prices are one of the most affordable on the market, and there are no hidden fees.

Instead, we offer bonuses, discounts, and free services to make your experience outstanding.
Sign up, place your order, and leave the rest to our professional paper writers in less than 2 minutes.
step 1
Upload assignment instructions
Fill out the order form and provide paper details. You can even attach screenshots or add additional instructions later. If something is not clear or missing, the writer will contact you for clarification.
s
Get personalized services with MyCoursebay
One writer for all your papers
You can select one writer for all your papers. This option enhances the consistency in the quality of your assignments. Select your preferred writer from the list of writers who have handledf your previous assignments
Same paper from different writers
Are you ordering the same assignment for a friend? You can get the same paper from different writers. The goal is to produce 100% unique and original papers
Copy of sources used
Our homework writers will provide you with copies of sources used on your request. Just add the option when plaing your order
What our partners say about us
We appreciate every review and are always looking for ways to grow. See what other students think about our do my paper service.
Other
I appreciate your work. Thank you????
Customer 452949, September 15th, 2023
Technology
Excellent job on the paper!
Customer 452885, December 28th, 2022
Criminal Justice
always great!
Customer 452465, February 23rd, 2021
Business and administrative studies
Perfect as always!
Customer 452909, April 15th, 2023
Mental Wellness
The skilled writer did a good job. I will add a few more details. Thank you, great job...
Customer 452547, June 17th, 2021
Nursing
Perfect as usual!!! Thanks team!
Customer 452453, May 26th, 2021
Human Resources Management (HRM)
Thank you so much.
Customer 452701, June 28th, 2023
Human Resources Management (HRM)
Great Paper!
Customer 452701, August 1st, 2023
Medicine
Great job! Thank you.
Customer 452707, May 29th, 2022
Human Resources Management (HRM)
Thank you.
Customer 452701, April 24th, 2023
Human Resources Management (HRM)
You did an awesome job with this paper. Thanks for the prompt delivery.
Customer 452701, October 24th, 2023
Nursing
Great writer (Proske). I highly recommend
Customer 452531, July 10th, 2021
OUR GIFT TO YOU
15% OFF your first order
Use a coupon FIRST15 and enjoy expert help with any task at the most affordable price.
Claim my 15% OFF Order in Chat

Good News ! We now help with PROCTORED EXAM. Chat with a support agent for more information

NEW

Thank you for choosing MyCoursebay. Your presence is a motivation to us. All papers are written from scratch. Plagiarism is not tolerated. Order now for a 15% discount

Order Now