{"id":21325,"date":"2025-11-17T01:45:45","date_gmt":"2025-11-16T22:45:45","guid":{"rendered":"https:\/\/hastane.ksu.edu.tr\/hastaliklar\/familial-hypocalciuric-hypercalcemia\/"},"modified":"2025-11-17T01:45:45","modified_gmt":"2025-11-16T22:45:45","slug":"familial-hypocalciuric-hypercalcemia","status":"publish","type":"hastaliklar","link":"https:\/\/hastane.ksu.edu.tr\/en\/hastaliklar\/familial-hypocalciuric-hypercalcemia\/","title":{"rendered":"Familial Hypocalciuric Hypercalcemia (FHH)"},"content":{"rendered":"<h2>Definition<\/h2>\n<p>Familial hypocalciuric hypercalcemia (FHH) is a benign autosomal dominant disease characterized by mild hypercalcemia and hypocalciuria, which develops due to a defect in the calcium sensing receptor (CaSR).<\/p>\n<h2>Symptoms<\/h2>\n<ul>\n<li>Usually asymptomatic<\/li>\n<li>Mild hypercalcemia<\/li>\n<li>Low urine calcium<\/li>\n<li>Similar history in family<\/li>\n<\/ul>\n<h2>Reasons<\/h2>\n<p>Heterozygous inactivating mutation in the calcium-sensing receptor (CaSR) gene.<\/p>\n<h2>Diagnosis<\/h2>\n<p>Slightly elevated blood calcium, low urinary calcium excretion, CaSR gene analysis.<\/p>\n<h2>Treatment<\/h2>\n<p>Treatment is usually not required. Parathyroidectomy should be avoided.<\/p>\n<h2>Which Polyclinic Should You Apply To?<\/h2>\n<p><strong>Endocrinology Polyclinic<\/strong><\/p>\n<h2>What to Do in an Emergency?<\/h2>\n<p>In rare cases, if a hypercalcemia crisis occurs, 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 Familial hypocalciuric hypercalcemia (FHH) is an autosomal dominant benign disease characterized by mild hypercalcemia and hypocalciuria, resulting from a defect in the calcium sensing receptor (CaSR). Symptoms Usually asymptomatic Mild hypercalcemia Low urinary calcium Family history of similar conditions Causes Heterozygous inactivating mutation in the calcium sensing receptor (CaSR) gene. Diagnosis Mildly elevated blood calcium, low urinary calcium excretion, [\u2026]<\/p>","protected":false},"author":1,"featured_media":0,"menu_order":0,"template":"","format":"standard","meta":{"_acf_changed":false,"slim_seo":{"title":"Familial Hypocalciuric Hypercalcemia (FHH) - Kahramanmara\u015f S\u00fct\u00e7\u00fc \u0130mam University Health Practice and Research Hospital","description":"Definition: Familial hypocalciuric hypercalcemia (FHH) is a disease characterized by mild hypercalcemia and hypocalciuria, resulting from a defect in the calcium sensing receptor (CaSR)."},"footnotes":""},"class_list":["post-21325","hastaliklar","type-hastaliklar","status-publish","format-standard","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/hastaliklar\/21325","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\/21325\/revisions"}],"wp:attachment":[{"href":"https:\/\/hastane.ksu.edu.tr\/en\/wp-json\/wp\/v2\/media?parent=21325"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}