{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,22]],"date-time":"2026-09-22T22:00:36Z","timestamp":1790114436428,"version":"4.0.1"},"reference-count":10,"publisher":"Oxford University Press (OUP)","issue":"8","license":[{"start":{"date-parts":[[2026,2,24]],"date-time":"2026-02-24T00:00:00Z","timestamp":1771891200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"funder":[{"name":"Research on Intractable Diseases Related to Disorders in Hormone Secretion and Action","award":["24FC1015"],"award-info":[{"award-number":["24FC1015"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,7,24]]},"abstract":"<jats:title>Vignette<\/jats:title>\n                  <jats:p>A 28-day-old female infant presented with clonic seizures secondary to hypocalcemia (calcium [Ca], 5.7\u00a0mg\/dL) and hypoparathyroidism (intact PTH, 7\u00a0pg\/mL). Despite the initiation of oral alfacalcidol therapy, she experienced recurrent episodes of generalized convulsions or focal tetany, despite calcium lactate administration during febrile episodes. Her younger sister exhibited frequent irritability until day 38 of life due to hypocalcemia (Ca, 7.7\u00a0mg\/dL) and hypoparathyroidism (intact PTH, 5\u00a0pg\/mL). She experienced 3 febrile generalized seizures during infancy despite oral alfacalcidol treatment. Both sisters developed nephrocalcinosis despite oral hydrochlorothiazide treatment to reduce hypercalciuria. Genetic testing identified a pathogenic variant, c.2504C&amp;gt;A (p.Ala835Asp), in the calcium-sensing receptor (CASR) gene in both sisters. Their father carried the same variant but remained asymptomatic. This finding led to a diagnosis of autosomal dominant hypocalcemia type 1 (ADH1). Optimal active vitamin D treatment in ADH1 remains challenging because of difficulty maintaining stable serum Ca levels amid fluctuating physiological demands, as well as persistent hypercalciuria resulting from combined PTH deficiency and CaSR activation. Emerging therapies, including calcilytics, may help to address these limitations.<\/jats:p>","DOI":"10.1093\/jbmr\/zjag034","type":"journal-article","created":{"date-parts":[[2026,2,23]],"date-time":"2026-02-23T12:25:33Z","timestamp":1771849533000},"page":"793-798","source":"Crossref","is-referenced-by-count":2,"title":["Autosomal dominant hypocalcemia type 1: status quo of tailored management and future perspectives"],"prefix":"10.1093","volume":"41","author":[{"given":"Daisuke","family":"Harada","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Osaka Hospital, Japan Community Healthcare Organization (JCHO) , Osaka 553-0003 ,","place":["Japan"]},{"name":"Department of Human Education, Faculty of Human Education, Momoyama Gakuin University , Izumi 594-1198 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