{"id":13762,"date":"2025-01-14T04:40:04","date_gmt":"2025-01-14T04:40:04","guid":{"rendered":"https:\/\/www.info-welt.com\/en\/index.php\/2025\/01\/14\/understanding-cystic-fibrosis-causes-and-treatment\/"},"modified":"2025-01-14T04:40:04","modified_gmt":"2025-01-14T04:40:04","slug":"understanding-cystic-fibrosis-causes-and-treatment","status":"publish","type":"post","link":"https:\/\/www.info-welt.com\/en\/index.php\/2025\/01\/14\/understanding-cystic-fibrosis-causes-and-treatment\/","title":{"rendered":"Understanding Cystic Fibrosis: Causes and Treatment"},"content":{"rendered":"<p><b>Cystic fibrosis<\/b> (CF) is a complex <b>genetic disorder<\/b> affecting thousands of U.S. families. It impacts multiple body systems, causing <b>mucus buildup<\/b> in vital organs. Over 40,000 children and adults in America live with this <b>respiratory disease<\/b><sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.cff.org\/intro-cf\/about-cystic-fibrosis\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">1<\/a><\/sup>.<\/p>\n<p>CF stems from a defective gene passed through generations. It mainly affects white people of North European ancestry<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.mayoclinic.org\/diseases-conditions\/cystic-fibrosis\/symptoms-causes\/syc-20353700\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">2<\/a><\/sup>. The condition creates thick, sticky secretions that block essential bodily pathways.<\/p>\n<p>Medical advances have greatly improved life expectancy for CF patients. Today, those diagnosed may live into their mid to late 50s<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.mayoclinic.org\/diseases-conditions\/cystic-fibrosis\/symptoms-causes\/syc-20353700\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">2<\/a><\/sup>. This is due to innovative screening techniques and targeted treatments.<\/p>\n<p>About 1,000 new CF cases are diagnosed yearly in the U.S. More than 75% of patients are identified by age two<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.cff.org\/intro-cf\/about-cystic-fibrosis\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">1<\/a><\/sup>. Early diagnosis is crucial for effective management of the condition.<\/p>\n<h3>Key Takeaways<\/h3>\n<ul>\n<li>CF is a <b>genetic disorder<\/b> affecting multiple body systems<\/li>\n<li>Over 40,000 Americans currently live with <b>cystic fibrosis<\/b><\/li>\n<li>Early diagnosis is crucial for effective management<\/li>\n<li>Medical treatments have significantly extended life expectancy<\/li>\n<li>Genetic screening helps identify the condition early<\/li>\n<\/ul>\n<h2>What is Cystic Fibrosis?<\/h2>\n<p><b>Cystic fibrosis<\/b> (CF) is a complex genetic condition affecting multiple body systems. It creates thick, sticky mucus that damages various organs. This inherited disorder poses significant challenges for those diagnosed<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.lung.org\/lung-health-diseases\/lung-disease-lookup\/cystic-fibrosis\/learn-about-cystic-fibrosis\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">3<\/a><\/sup>.<\/p>\n<h3>Understanding the Condition<\/h3>\n<p>CF results from specific genetic mutations in the <b>CFTR gene<\/b>. These mutations cause abnormal protein production, leading to critical health complications<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.lung.org\/lung-health-diseases\/lung-disease-lookup\/cystic-fibrosis\/learn-about-cystic-fibrosis\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">3<\/a><\/sup>.<\/p>\n<p>About 40,000 people in the United States live with CF. Approximately 1 in 30 people are genetic carriers<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.lung.org\/lung-health-diseases\/lung-disease-lookup\/cystic-fibrosis\/learn-about-cystic-fibrosis\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">3<\/a><\/sup>.<\/p>\n<h3>Body System Impacts<\/h3>\n<ul>\n<li>Lungs: Creates thick mucus causing persistent <b>lung infections<\/b><\/li>\n<li>Pancreas: Leads to <b>pancreatic insufficiency<\/b> and <b>malnutrition<\/b><\/li>\n<li>Digestive system: Impairs nutrient absorption<\/li>\n<\/ul>\n<h3>Common Symptoms<\/h3>\n<p>People with CF experience various symptoms that progressively affect their health. Key indicators include:<\/p>\n<ol>\n<li>Persistent coughing with thick mucus<\/li>\n<li>Frequent <b>lung infections<\/b><\/li>\n<li>Salty-tasting skin<\/li>\n<li>Poor growth and weight gain<\/li>\n<\/ol>\n<blockquote><p>\\&#8221;Early detection and comprehensive management are crucial for improving <b>quality of life<\/b> with cystic fibrosis.\\&#8221;<\/p><\/blockquote>\n<table>\n<tr>\n<th>Body System<\/th>\n<th>CF Impact<\/th>\n<\/tr>\n<tr>\n<td>Respiratory<\/td>\n<td>Chronic <b>lung infections<\/b>, reduced lung function<\/td>\n<\/tr>\n<tr>\n<td>Digestive<\/td>\n<td><b>Pancreatic insufficiency<\/b>, <b>malnutrition<\/b> risks<\/td>\n<\/tr>\n<tr>\n<td>Reproductive<\/td>\n<td>Male infertility potential<\/td>\n<\/tr>\n<\/table>\n<p>Managing CF requires comprehensive medical care and ongoing strategies. Treatments aim to improve breathing and prevent infections. They also support nutritional needs<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.hopkinsmedicine.org\/health\/conditions-and-diseases\/cystic-fibrosis\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">4<\/a><\/sup><sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.cdc.gov\/cystic-fibrosis\/about\/index.html\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">5<\/a><\/sup>.<\/p>\n<h2>Causes of Cystic Fibrosis<\/h2>\n<p>Cystic fibrosis is a complex <b>inherited condition<\/b>. Genetic factors play a key role in its development. Understanding these causes helps grasp how the disease impacts individuals.<\/p>\n<h3>Genetic Foundations<\/h3>\n<p>A specific <b>CFTR gene mutation<\/b> causes cystic fibrosis. It follows an <b>autosomal recessive inheritance<\/b> pattern. <em>This means both parents must carry at least one copy of the defective gene<\/em> for a child to potentially develop the condition<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.cff.org\/intro-cf\/cf-genetics-basics\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">6<\/a><\/sup>.<\/p>\n<ul>\n<li>About 10 million Americans are CF gene carriers<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.cff.org\/intro-cf\/cf-genetics-basics\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">6<\/a><\/sup><\/li>\n<li>When two carriers have a child, there\\&#8217;s a 25% chance the child will have CF<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.cff.org\/intro-cf\/cf-genetics-basics\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">6<\/a><\/sup><\/li>\n<li>Approximately 30,000 people in the United States live with cystic fibrosis<sup class=\\\"citation\\\"><a href=\\\"https:\/\/emedicine.medscape.com\/article\/1001602-overview\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">7<\/a><\/sup><\/li>\n<\/ul>\n<p><div class=\"ast-oembed-container \" style=\"height: 100%;\"><iframe loading=\"lazy\" title=\"Cystic Fibrosis (CF): Symptoms, Inheritance, Treatment, and More | Mass General Brigham\" width=\"500\" height=\"281\" src=\"https:\/\/www.youtube.com\/embed\/YpZdRRjbpi8?feature=oembed\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture; web-share\" referrerpolicy=\"strict-origin-when-cross-origin\" allowfullscreen><\/iframe><\/div>\n<\/p>\n<h3>Prevalence and Demographics<\/h3>\n<p>Cystic fibrosis affects different populations uniquely. In the United States, it impacts about 1 in 2,500 to 3,500 white newborns. Other ethnic groups have lower rates<sup class=\\\"citation\\\"><a href=\\\"https:\/\/medlineplus.gov\/genetics\/condition\/cystic-fibrosis\/\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">8<\/a><\/sup>.<\/p>\n<h3>Common Misconceptions<\/h3>\n<p>Many people misunderstand cystic fibrosis. It\\&#8217;s not just a lung disease. CF is a complex genetic condition affecting multiple organ systems.<\/p>\n<p>Symptom severity can vary among individuals. This adds to the complexity of the disease.<\/p>\n<blockquote><p>Genetic knowledge is power when understanding inherited conditions like cystic fibrosis.<\/p><\/blockquote>\n<p>Knowing your genetic risk is crucial. It helps make informed decisions about family planning. It also aids in considering potential screening options.<\/p>\n<h2>Treatment Options for Cystic Fibrosis<\/h2>\n<p>Cystic fibrosis management requires a holistic approach. Your treatment plan will be customized to your specific symptoms and health needs<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.nhs.uk\/conditions\/cystic-fibrosis\/treatment\/\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">9<\/a><\/sup>.<\/p>\n<p>New treatments have greatly improved life for those with cystic fibrosis<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.lung.org\/lung-health-diseases\/lung-disease-lookup\/cystic-fibrosis\/treating-and-managing\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">10<\/a><\/sup>. The main goal is to manage symptoms and prevent complications through various methods.<\/p>\n<h3>Innovative Medications and Therapies<\/h3>\n<p><b>CFTR modulators<\/b> have transformed treatment by targeting the genetic protein defect. Patients 12 and older can use combo medicines like Kaftrio<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.nhs.uk\/conditions\/cystic-fibrosis\/treatment\/\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">9<\/a><\/sup>.<\/p>\n<ul>\n<li>Dornase alfa helps thin lung mucus<\/li>\n<li>Hypertonic saline improves mucus clearance<\/li>\n<li>Ivacaftor and lumacaftor reduce mucus levels<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.nhs.uk\/conditions\/cystic-fibrosis\/treatment\/\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">9<\/a><\/sup><\/li>\n<\/ul>\n<h3>Airway Clearance Techniques<\/h3>\n<p>Managing lung issues requires special airway clearing methods. Physiotherapists can teach you techniques like ACBT to keep your lungs clear<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.nhs.uk\/conditions\/cystic-fibrosis\/treatment\/\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">9<\/a><\/sup>.<\/p>\n<blockquote><p>\\&#8221;Physical activities like swimming and running can help clear mucus and enhance overall health\\&#8221;<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.nhs.uk\/conditions\/cystic-fibrosis\/treatment\/\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">9<\/a><\/sup><\/p><\/blockquote>\n<h3>Nutritional Support and Ongoing Care<\/h3>\n<p>Proper nutrition is vital for people with cystic fibrosis. Enzyme replacements help you absorb nutrients, while a high-calorie diet supports overall health<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.lung.org\/lung-health-diseases\/lung-disease-lookup\/cystic-fibrosis\/treating-and-managing\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">10<\/a><\/sup>.<\/p>\n<p>Your care may include <a href=\\\"https:\/\/www.mayoclinic.org\/diseases-conditions\/cystic-fibrosis\/diagnosis-treatment\/drc-20353706\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">regular check-ups<\/a>, vaccinations, and a healthcare team to monitor your condition<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.lung.org\/lung-health-diseases\/lung-disease-lookup\/cystic-fibrosis\/treating-and-managing\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">10<\/a><\/sup>.<\/p>\n<h2>Living with Cystic Fibrosis<\/h2>\n<p>Cystic fibrosis (CF) care has improved significantly. People with CF now live longer, more fulfilling lives. Effective health management involves proper nutrition, consistent medical care, and smart lifestyle choices<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.cff.org\/managing-cf\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">11<\/a><\/sup>.<\/p>\n<p>CF doesn\\&#8217;t limit your experiences. With planning, you can travel, study, and build relationships. <a href=\\\"https:\/\/health.choc.org\/life-with-cystic-fibrosis\/\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">Specialized CF care centers<\/a> offer vital support and resources<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.cff.org\/managing-cf\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">11<\/a><\/sup>.<\/p>\n<p>These centers provide comprehensive care beyond medical treatment. They focus on your overall well-being. Support networks are crucial in managing CF.<\/p>\n<p>Family, friends, and community groups offer emotional and practical help. The CF <b>patient registry<\/b> tracks treatment progress. It also aids in developing new therapies<sup class=\\\"citation\\\"><a href=\\\"https:\/\/www.cff.org\/support\/coping-while-caring-someone-cystic-fibrosis\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">12<\/a><\/sup>.<\/p>\n<p>Your CF diagnosis doesn\\&#8217;t define you. Embrace comprehensive care strategies and maintain strong support systems. Focus on personal goals to lead a vibrant life.<\/p>\n<p>Each day offers chances to thrive and create meaningful experiences. Remember, you\\&#8217;re more than your medical condition.<\/p>\n<section class=\\\"schema-section\\\">\n<h2>FAQ<\/h2>\n<div>\n<h3>What is Cystic Fibrosis?<\/h3>\n<div>\n<div>\n<p>Cystic Fibrosis (CF) is a <b>genetic disorder<\/b> affecting about 40,000 people in the United States. It causes thick <b>mucus buildup<\/b> in organs, mainly the lungs and pancreas. This results from mutations in the <b>CFTR gene<\/b>, leading to respiratory and digestive problems.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<div>\n<h3>How is Cystic Fibrosis inherited?<\/h3>\n<div>\n<div>\n<p>CF is inherited when both parents carry a defective <b>CFTR gene<\/b>. Over 1,700 known mutations of this gene exist. If both parents are carriers, there\\&#8217;s a 25% chance their child will have CF.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<div>\n<h3>What are the main symptoms of Cystic Fibrosis?<\/h3>\n<div>\n<div>\n<p>Common symptoms include persistent coughing with phlegm and frequent lung infections. You might also experience salty-tasting skin, poor growth, and digestive issues. Chronic sinus infections and nasal polyps are possible.<\/p>\n<p>Symptoms can vary widely between individuals due to different gene mutations. Males may face potential fertility issues.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<div>\n<h3>How is Cystic Fibrosis diagnosed?<\/h3>\n<div>\n<div>\n<p>Diagnosis involves newborn screening, sweat tests, and genetic testing. Comprehensive clinical evaluation at specialized <b>CF care centers<\/b> is also crucial. Early detection allows for immediate treatment and better management.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<div>\n<h3>What treatment options are available?<\/h3>\n<div>\n<div>\n<p>Treatment is personalized and includes <b>airway clearance techniques<\/b> and inhaled medications. Pancreatic enzyme supplements and nutritional support are often necessary. <b>CFTR modulators<\/b> have improved treatment by targeting the underlying protein defect.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<div>\n<h3>Can people with Cystic Fibrosis live a normal life?<\/h3>\n<div>\n<div>\n<p>Yes, many people with CF lead fulfilling lives with proper care. Medical advances have improved life expectancy and <b>quality of life<\/b>. Daily management and support networks are key to effective disease control.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<div>\n<h3>Is there a cure for Cystic Fibrosis?<\/h3>\n<div>\n<div>\n<p>Currently, there\\&#8217;s no complete cure, but research continues to develop new therapies. The Cystic Fibrosis Foundation supports extensive research for better treatments. <b>CFTR modulators<\/b> have already made significant improvements in disease management.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<div>\n<h3>How does Cystic Fibrosis affect the digestive system?<\/h3>\n<div>\n<div>\n<p>CF can cause <b>pancreatic insufficiency<\/b>, reducing digestive enzyme production. This leads to nutrient absorption issues and potential <b>malnutrition<\/b>. Patients often need enzyme supplements with meals to help digest food properly.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<div>\n<h3>What support is available for people with Cystic Fibrosis?<\/h3>\n<div>\n<div>\n<p>The Cystic Fibrosis Foundation accredits over 130 specialized care centers. It provides support networks and resources for patients and families. These systems help manage physical and emotional challenges, connecting individuals with experts and peer groups.<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/section>\n<h2>Source Links<\/h2>\n<ol data-type=\\\"sources\\\">\n<li>About Cystic Fibrosis &#8211; <a href=\\\"https:\/\/www.cff.org\/intro-cf\/about-cystic-fibrosis\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">https:\/\/www.cff.org\/intro-cf\/about-cystic-fibrosis<\/a><\/li>\n<li>Cystic fibrosis &#8211; Symptoms and causes &#8211; <a href=\\\"https:\/\/www.mayoclinic.org\/diseases-conditions\/cystic-fibrosis\/symptoms-causes\/syc-20353700\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">https:\/\/www.mayoclinic.org\/diseases-conditions\/cystic-fibrosis\/symptoms-causes\/syc-20353700<\/a><\/li>\n<li>Learn About Cystic Fibrosis &#8211; <a href=\\\"https:\/\/www.lung.org\/lung-health-diseases\/lung-disease-lookup\/cystic-fibrosis\/learn-about-cystic-fibrosis\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">https:\/\/www.lung.org\/lung-health-diseases\/lung-disease-lookup\/cystic-fibrosis\/learn-about-cystic-fibrosis<\/a><\/li>\n<li>Cystic Fibrosis &#8211; <a href=\\\"https:\/\/www.hopkinsmedicine.org\/health\/conditions-and-diseases\/cystic-fibrosis\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">https:\/\/www.hopkinsmedicine.org\/health\/conditions-and-diseases\/cystic-fibrosis<\/a><\/li>\n<li>About Cystic Fibrosis &#8211; <a href=\\\"https:\/\/www.cdc.gov\/cystic-fibrosis\/about\/index.html\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">https:\/\/www.cdc.gov\/cystic-fibrosis\/about\/index.html<\/a><\/li>\n<li>CF Genetics: The Basics &#8211; <a href=\\\"https:\/\/www.cff.org\/intro-cf\/cf-genetics-basics\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">https:\/\/www.cff.org\/intro-cf\/cf-genetics-basics<\/a><\/li>\n<li>Cystic Fibrosis: Practice Essentials, Background, Pathophysiology &#8211; <a href=\\\"https:\/\/emedicine.medscape.com\/article\/1001602-overview\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">https:\/\/emedicine.medscape.com\/article\/1001602-overview<\/a><\/li>\n<li>Cystic fibrosis: MedlinePlus Genetics &#8211; <a href=\\\"https:\/\/medlineplus.gov\/genetics\/condition\/cystic-fibrosis\/\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">https:\/\/medlineplus.gov\/genetics\/condition\/cystic-fibrosis\/<\/a><\/li>\n<li>Cystic fibrosis &#8211; Treatment &#8211; <a href=\\\"https:\/\/www.nhs.uk\/conditions\/cystic-fibrosis\/treatment\/\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">https:\/\/www.nhs.uk\/conditions\/cystic-fibrosis\/treatment\/<\/a><\/li>\n<li>Diagnosing and Treating Cystic Fibrosis &#8211; <a href=\\\"https:\/\/www.lung.org\/lung-health-diseases\/lung-disease-lookup\/cystic-fibrosis\/treating-and-managing\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">https:\/\/www.lung.org\/lung-health-diseases\/lung-disease-lookup\/cystic-fibrosis\/treating-and-managing<\/a><\/li>\n<li>Managing CF &#8211; <a href=\\\"https:\/\/www.cff.org\/managing-cf\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">https:\/\/www.cff.org\/managing-cf<\/a><\/li>\n<li>Coping While Caring for Someone With Cystic Fibrosis &#8211; <a href=\\\"https:\/\/www.cff.org\/support\/coping-while-caring-someone-cystic-fibrosis\\\" target=\\\"_blank\\\" rel=\\\"nofollow\\\">https:\/\/www.cff.org\/support\/coping-while-caring-someone-cystic-fibrosis<\/a><\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>Learn about cystic fibrosis, its genetic causes, symptoms, and modern treatments. Discover how this inherited condition affects the lungs and digestive system, and explore management options<\/p>\n","protected":false},"author":1,"featured_media":13764,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_uag_custom_page_level_css":"","site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[5],"tags":[571,876,877,579,878,879,880,881],"class_list":["post-13762","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-health","tag-chronic-illness","tag-cystic-fibrosis-causes","tag-cystic-fibrosis-treatment","tag-genetic-disorders","tag-genetic-testing","tag-lung-health","tag-pulmonary-function","tag-respiratory-system"],"uagb_featured_image_src":{"full":false,"thumbnail":false,"medium":false,"medium_large":false,"large":false,"1536x1536":false,"2048x2048":false},"uagb_author_info":{"display_name":"wpmanag984","author_link":"https:\/\/www.info-welt.com\/en\/author\/wpmanag984\/"},"uagb_comment_info":0,"uagb_excerpt":"Learn about cystic fibrosis, its genetic causes, symptoms, and modern treatments. Discover how this inherited condition affects the lungs and digestive system, and explore management options","_links":{"self":[{"href":"https:\/\/www.info-welt.com\/en\/index.php\/wp-json\/wp\/v2\/posts\/13762","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.info-welt.com\/en\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.info-welt.com\/en\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.info-welt.com\/en\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.info-welt.com\/en\/index.php\/wp-json\/wp\/v2\/comments?post=13762"}],"version-history":[{"count":0,"href":"https:\/\/www.info-welt.com\/en\/index.php\/wp-json\/wp\/v2\/posts\/13762\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.info-welt.com\/en\/index.php\/wp-json\/wp\/v2\/media?parent=13762"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.info-welt.com\/en\/index.php\/wp-json\/wp\/v2\/categories?post=13762"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.info-welt.com\/en\/index.php\/wp-json\/wp\/v2\/tags?post=13762"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}