{"id":21320,"date":"2025-11-17T01:45:45","date_gmt":"2025-11-16T22:45:45","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/bartter-sendromu\/"},"modified":"2025-11-17T01:45:45","modified_gmt":"2025-11-16T22:45:45","slug":"bartter-sendromu","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/bartter-sendromu\/","title":{"rendered":"Bartter Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Bartter syndrome is a rare autosomal recessive renal tubulopathy characterized by sodium and chloride malabsorption in the thick ascending limb of the loop of Henle.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Polyuria, polydipsia<\/li>\n<li>Growth retardation<\/li>\n<li>Muscle weakness<\/li>\n<li>Dehydration<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>Mutation in genes encoding ion channel proteins in the ascending limb of the loop of Henle.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Low blood potassium and chloride, metabolic alkalosis, high plasma renin and aldosterone.<\/p>\n<h2>Treatment<\/h2>\n<p>Potassium supplements, NSAIDs (indomethacin), ACE inhibitors.<\/p>\n<h2>Which Polyclinic Should You Apply To?<\/h2>\n<p><strong>Pediatric Nephrology Outpatient Clinic<\/strong> or <strong>Nephrology Polyclinic<\/strong><\/p>\n<h2>What to Do in an Emergency?<\/h2>\n<p>In case of severe dehydration or hypokalemic paralysis, 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 Bartter syndrome is a rare, autosomal recessive renal tubulopathy characterized by impaired sodium and chloride absorption in the thick ascending limb of the loop of Henle. Symptoms Polyuria, polydipsia Growth retardation Muscle weakness Dehydration Causes Mutations in genes encoding ion channel proteins in the ascending limb of the loop of Henle. Diagnosis Low potassium and chloride levels in the blood, metabolic alkalosis, high plasma renin and aldosterone. Treatment [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Bartter Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Bartter syndrome is a rare, autosomal recessive renal tubulopathy characterized by impaired sodium and chloride absorption in the thick ascending limb of the loop of Henle."},"footnotes":""},"class_list":["post-21320","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21320","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\/21320\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21320"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}