{"id":21562,"date":"2025-11-17T04:06:05","date_gmt":"2025-11-17T01:06:05","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/alpha-1-antitripsin-eksikligi\/"},"modified":"2025-11-17T04:06:05","modified_gmt":"2025-11-17T01:06:05","slug":"alpha-1-antitripsin-eksikligi","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/alpha-1-antitripsin-eksikligi\/","title":{"rendered":"Alpha-1 Antitrypsin Deficiency"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Alpha-1 antitrypsin deficiency is an inherited metabolic disease that causes damage to the liver and lungs.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Shortness of breath<\/li>\n<li>Jaundice<\/li>\n<li>Liver failure<\/li>\n<li>Early emphysema<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>SERPINA1 gene mutation.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Alpha-1 antitrypsin level, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Alpha-1 antitrypsin replacement, supportive care.<\/p>\n<h2>Which Polyclinic Should You Apply To?<\/h2>\n<p><strong>Chest Diseases Polyclinic<\/strong><\/p>\n<h2>What to Do in an Emergency?<\/h2>\n<p>In case of respiratory failure, emergency services should be consulted.<\/p>\n<p><em>This page is for general information purposes only.<\/em><\/p>","protected":false},"excerpt":{"rendered":"<p>Definition: Alpha-1 antitrypsin deficiency is a hereditary metabolic disease that causes damage to the liver and lungs. Symptoms: Shortness of breath, jaundice, liver failure, early emphysema. Causes: SERPINA1 gene mutation. Diagnosis: Alpha-1 antitrypsin level, genetic testing. Treatment: Alpha-1 antitrypsin replacement, supportive therapy. Which Clinic Should You Go To? Pulmonology Clinic. What to Do in an Emergency? In case of respiratory failure, go to the emergency room. This [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Alpha-1 Antitrypsin Deficiency - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Alpha-1 antitrypsin deficiency is a hereditary metabolic disorder that causes damage to the liver and lungs. Symptoms: Shortness of breath, jaundice, liver damage."},"footnotes":""},"class_list":["post-21562","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21562","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar"}],"about":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/types\/hastaliklar"}],"author":[{"embeddable":true,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/users\/1"}],"version-history":[{"count":0,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21562\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21562"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}