{"id":21260,"date":"2025-11-17T01:45:43","date_gmt":"2025-11-16T22:45:43","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/galactosemia\/"},"modified":"2025-11-17T01:45:43","modified_gmt":"2025-11-16T22:45:43","slug":"galactosemia","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/galactosemia\/","title":{"rendered":"Galactosemia"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Galactosemia is a metabolic disease characterized by galactose-1-phosphate uridyl transferase enzyme deficiency, which presents with sepsis-like symptoms in the neonatal period and long-term complications.<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Sepsis-like picture in the newborn<\/li>\n<li>Liver failure<\/li>\n<li>Cataract<\/li>\n<li>Developmental delay<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>GALT gene mutation.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Newborn screening, enzyme activity.<\/p>\n<h2>Treatment<\/h2>\n<p>Galacto-free diet.<\/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 sepsis-like condition, 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: Galactosemia is a metabolic disease characterized by galactose-1-phosphate uridyltransferase enzyme deficiency, presenting with sepsis-like symptoms in the neonatal period and long-term complications. Symptoms: Sepsis-like symptoms in newborns, liver failure, cataracts, developmental delay. Causes: GALT gene mutation. Diagnosis: Neonatal screening, enzyme activity. Treatment: Galactose-free diet. Which Clinic to Consult? Metabolism Clinic. What to Do in an Emergency? Sepsis [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Galactosemia - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Galactosemia is a disease characterized by galactose-1-phosphate uridyltransferase enzyme deficiency, presenting with a sepsis-like picture in the neonatal period and long-term complications."},"footnotes":""},"class_list":["post-21260","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21260","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\/21260\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21260"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}