{"id":21259,"date":"2025-11-17T01:45:43","date_gmt":"2025-11-16T22:45:43","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/fanconi-bickel\/"},"modified":"2025-11-17T01:45:43","modified_gmt":"2025-11-16T22:45:43","slug":"fanconi-bickel","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/fanconi-bickel\/","title":{"rendered":"Fanconi-Bickel Syndrome"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Fanconi-Bickel syndrome is a rare metabolic disease characterized by GLUT2 transporter defect, accompanied by hepatorenal glycogen storage and renal Fanconi syndrome.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Hepatomegaly<\/li>\n<li>Renal Fanconi syndrome<\/li>\n<li>Growth retardation<\/li>\n<li>Rickets<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>SLC2A2 gene mutation.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Genetic testing, biochemical tests.<\/p>\n<h2>Treatment<\/h2>\n<p>Symptomatic treatment.<\/p>\n<h2>Which Polyclinic Should You Apply To?<\/h2>\n<p><strong>Metabolism Polyclinic<\/strong><\/p>\n<h2>What to Do in an Emergency?<\/h2>\n<p>In case of dehydration, 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: Fanconi-Bickel syndrome is a rare metabolic disease characterized by a GLUT2 transporter defect, hepatorenal glycogen storage, and renal Fanconi syndrome. Symptoms: Hepatomegaly, Renal Fanconi syndrome, Growth retardation, Rickets. Causes: SLC2A2 gene mutation. Diagnosis: Genetic testing, biochemical tests. Treatment: Symptomatic treatment. Which Clinic Should You Go To? Metabolism Clinic. What to Do in an Emergency? In case of dehydration, go to the emergency room. [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Fanconi-Bickel Syndrome - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Fanconi-Bickel syndrome is a rare metastatic disease characterized by a GLUT2 transporter defect, hepatorenal glycogen storage, and renal Fanconi syndrome."},"footnotes":""},"class_list":["post-21259","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21259","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\/21259\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21259"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}