{"id":21181,"date":"2025-11-17T01:45:45","date_gmt":"2025-11-16T22:45:45","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/bardet-biedl\/"},"modified":"2025-11-17T01:45:45","modified_gmt":"2025-11-16T22:45:45","slug":"bardet-biedl","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/bardet-biedl\/","title":{"rendered":"Bardet-Biedl Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Bardet-Biedl syndrome is an autosomal recessive ciliopathic disease characterized by obesity, retinal dystrophy, polydactyly, renal anomalies, hypogonadism and learning disabilities.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Obesity<\/li>\n<li>Retinitis pigmentosa (vision loss)<\/li>\n<li>Polydactyly (extra fingers)<\/li>\n<li>Kidney failure<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>Mutation in one of the BBS genes (ciliary dysfunction).<\/p>\n<h2>Diagnosis<\/h2>\n<p>Clinical criteria, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Symptomatic treatment (diet, vision rehabilitation, kidney therapy).<\/p>\n<h2>Which Polyclinic Should You Apply To?<\/h2>\n<p><strong>Genetics Polyclinic<\/strong> or <strong>Pediatric Nephrology Outpatient Clinic<\/strong><\/p>\n<h2>What to Do in an Emergency?<\/h2>\n<p>In case of renal failure or diabetic ketoacidosis, 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 Bardet-Biedl syndrome is an autosomal recessive ciliopathic disease characterized by obesity, retinal dystrophy, polydactyly, renal anomalies, hypogonadism, and learning disabilities. Symptoms Obesity Retinitis pigmentosa (vision loss) Polydactyly (extra fingers) Renal failure Causes Mutation in one of the BBS genes (ciliary dysfunction). Diagnosis Clinical criteria, genetic testing. Treatment Symptomatic treatment (diet, visual rehabilitation, renal treatment). Which Polyclinic [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Bardet-Biedl Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Bardet-Biedl syndrome is an autosomal recessive disorder characterized by obesity, retinal dystrophy, polydactyly, renal anomalies, hypogonadism, and learning disabilities."},"footnotes":""},"class_list":["post-21181","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21181","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":1,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21181\/revisions"}],"predecessor-version":[{"id":21341,"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21181\/revisions\/21341"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21181"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}