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Biol 2402 Cystic Fibrosis Research Paper

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This is a comprehensive and detailed research paper on Cystic Fibrosis. *Essential Study Material!!

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  • November 5, 2024
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Cystic Fibrosis 1




Cystic Fibrosis and the disease's harrowing toll

Kaitlyn Michele Schack

Lone Star College Montgomery

BIOL 2402: Anatomy and Physiology II

Professor Melissa Jackson

June 23, 2023

, Cystic Fibrosis 2




Introduction

Cystic Fibrosis, commonly known as CF, is a progressive, degenerative, chronic, and

often fatal disease affecting children and young adults. Cystic fibrosis mainly affects the lungs

but can affect ones digestive system as well. There have been many advancements in treats, so

over half the CF population has been living past 40 years! CF is when thick, rough, and heavy

mucous clogs and blocks the respiratory tracts and parts of the digestive system; this can lead to

infections, labored breathing, and weakening of the lungs; all in all, this causes irreversible

damage and will cause lungs to stop working partially or altogether leading to death. Patients

with CF now have higher chances of survival rates and tend to live longer than those who had it

decades ago due to the vast improvements in treatments.

Discussion

According to the National Library of Medicine, Cystic fibrosis (CF) is a genetic condition

that affects a protein in the body. Those with cystic fibrosis have a faulty protein that affects their

body’s cells, tissues, and glands that make mucus and sweat. People with cystic fibrosis make

thick, sticky mucus, as opposed to the thin and slippery mucous that no CF people make. The

thick and sticky mucus can build up, leading to blockages, damage, or infections in the affected

organs. Inflammation also causes damage to organs such as the lungs and pancreas.

According to Clevland Clinic, some of the most common symptoms include failure to

thrive, loose or oily stools, wheezing, a nagging cough, recurrent sinus infections, pneumonia, or

bronchitis. The Clevland Clinic stated different ways to test and diagnose CF, such as genetic

testing, newborn screening, Chest and Sinus X-rays, sputum cultures, or sweat tests. A sweat test

is a test that measures how much chloride and sodium are in the sweat. People with cystic

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