{"id":21235,"date":"2025-11-17T01:45:43","date_gmt":"2025-11-16T22:45:43","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/fabry\/"},"modified":"2025-11-17T01:45:43","modified_gmt":"2025-11-16T22:45:43","slug":"fabry","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/fabry\/","title":{"rendered":"Fabry Disease"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Fabry disease is a lysosomal storage disease characterized by pain, angiokeratomas, and multiorgan involvement, resulting from alpha-galactosidase A enzyme deficiency.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Burning pain attacks<\/li>\n<li>Angiokeratomas<\/li>\n<li>Kidney failure<\/li>\n<li>Cardiac involvement<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>GLA gene mutation.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Enzyme activity, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Enzyme replacement therapy.<\/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 a pain crisis, the emergency room should be consulted.<\/p>\n<p><em>This page is for general information purposes only.<\/em><\/p>","protected":false},"excerpt":{"rendered":"<p>Definition: Fabry disease is a lysosomal storage disease characterized by pain, angiokeratomas, and multiorgan involvement, resulting from alpha-galactosidase A enzyme deficiency. Symptoms: Burning pain attacks, angiokeratomas, kidney failure, cardiac involvement. Causes: GLA gene mutation. Diagnosis: Enzyme activity testing, genetic testing. Treatment: Enzyme replacement therapy. Which Clinic Should You Go To? Metabolism Clinic. What to Do in an Emergency? In case of a pain crisis, 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":"Fabry Disease - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Fabry disease is a lysosomal storage disorder resulting from alpha-galactosidase A enzyme deficiency, characterized by pain, angiokeratomas, and multiorgan involvement."},"footnotes":""},"class_list":["post-21235","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21235","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\/21235\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21235"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}