{"id":21237,"date":"2025-11-17T01:45:43","date_gmt":"2025-11-16T22:45:43","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/krabbe\/"},"modified":"2025-11-17T01:45:43","modified_gmt":"2025-11-16T22:45:43","slug":"krabbe","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/krabbe\/","title":{"rendered":"Krabbe Disease"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Krabbe disease is a lysosomal storage disease characterized by progressive neurological disorder and peripheral neuropathy, resulting from galactocerebrosidase enzyme deficiency.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Irritability<\/li>\n<li>Hypotonia<\/li>\n<li>Neurological decline<\/li>\n<li>Peripheral neuropathy<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>GALC gene mutation.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Enzyme activity, genetic testing.<\/p>\n<h2>Treatment<\/h2>\n<p>Bone marrow transplant.<\/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 status epilepticus, 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 Krabbe disease is a lysosomal storage disease characterized by progressive neurological impairment and peripheral neuropathy resulting from galactocerebrosidase enzyme deficiency. Symptoms Irritability Hypotonia Neurological regression Peripheral neuropathy Causes GALC gene mutation. Diagnosis Enzyme activity, genetic testing. Treatment Bone marrow transplant. Which Clinic Should You Go To? Metabolism Clinic What to Do in an Emergency? In case of status epilepticus, you should 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":"Krabbe Disease - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Krabbe disease is a lysosomal storage disorder characterized by progressive neurological impairment and peripheral neuropathy resulting from a deficiency of the galactocerebrosidase enzyme."},"footnotes":""},"class_list":["post-21237","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21237","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\/21237\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21237"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}