{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,7,3]],"date-time":"2025-07-03T06:40:05Z","timestamp":1751524805761,"version":"3.41.0"},"reference-count":19,"publisher":"Korean Society of Pediatric Nephrology","issue":"2","funder":[{"DOI":"10.13039\/501100002449","name":"Jeju National University","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100002449","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["chikd.org"],"crossmark-restriction":true},"short-container-title":["Child Kidney Dis"],"abstract":"<jats:p>Primary hyperparathyroidism (pHPT), an extremely rare condition observed in children, only has 2 to 5 reported cases per 100,000 individuals. This case involves a 13-year-old boy presenting with bilateral renal stones, significantly elevated calcium levels (13.0 mg\/dL), and a parathyroid hormone level of 296.2 pg\/mL (normal range, 10\u201365 pg\/mL). A parathyroid mass was identified through technetium-99m sestamibi scintigraphy. Pediatric cases of pHPT often involve nephrolithiasis, which is frequently linked to genetic conditions. Early and thorough metabolic evaluations are critical for accurate diagnosis and intervention, aiming to prevent serious long-term complications, such as chronic kidney disease and skeletal abnormalities. This case highlights the necessity of meticulous diagnostic protocols for nephrolithiasis in children.<\/jats:p>","DOI":"10.3339\/ckd.25.012","type":"journal-article","created":{"date-parts":[[2025,6,27]],"date-time":"2025-06-27T09:15:35Z","timestamp":1751015735000},"page":"83-88","update-policy":"https:\/\/doi.org\/10.3339\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Bilateral renal stones secondary to primary hyperparathyroidism in a 13-year-old boy: a case report"],"prefix":"10.3339","volume":"29","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6387-5803","authenticated-orcid":true,"given":"Yeonghoon","family":"Cho","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1234-5308","authenticated-orcid":true,"given":"Jungmin","family":"Ahn","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5327-0934","authenticated-orcid":true,"given":"Min-su","family":"Oh","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6830-7311","authenticated-orcid":true,"given":"Kyoung Hee","family":"Han","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1891","published-online":{"date-parts":[[2025,6,27]]},"reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1038\/ki.2011.336"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1016\/s0022-5347(17)59347-7"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1016\/s0022-3468(87)80438-4"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.5152\/tud.2020.20315"},{"key":"ref5","first-page":"234","volume-title":"Review of clinical characteristics of primary hyperparathyroidism: analysis of reported cases in Korea including recently experienced 17 cases","author":"Chung","year":"1992"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.6065\/apem.2019.24.3.195"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.6065\/apem.1938172.086"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.6065\/apem.2142006.003"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1016\/j.jcma.2012.06.012"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.5114\/pedm.2022.118315"},{"key":"ref11","first-page":"N44","volume-title":"Primary hyperparathyroidism in children and adolescents: the Johns Hopkins Children's Center experience 1984-2001","author":"Hsu","year":"2002"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1002\/jbmr.4665"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.1155\/2018\/3068365"},{"key":"ref14","doi-asserted-by":"publisher","DOI":"10.1186\/s12882-015-0126-1"},{"key":"ref15","doi-asserted-by":"publisher","DOI":"10.1016\/j.pcl.2012.05.009"},{"key":"ref16","doi-asserted-by":"publisher","DOI":"10.3390\/jcm13041114"},{"key":"ref17","doi-asserted-by":"publisher","DOI":"10.5489\/cuaj.7872"},{"key":"ref18","first-page":"94","volume-title":"Parathyroid adenoma in a child: a rare case report with cytomorphological clues","author":"Bhadarge","year":"2015"},{"key":"ref19","doi-asserted-by":"publisher","DOI":"10.1056\/nejmcp1106636"}],"container-title":["Childhood Kidney Diseases"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/chikd.org\/upload\/ckd-25-012.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,7,3]],"date-time":"2025-07-03T06:01:54Z","timestamp":1751522514000},"score":1,"resource":{"primary":{"URL":"http:\/\/chikd.org\/journal\/view.php?id=10.3339\/ckd.25.012"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,6,27]]},"references-count":19,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2025,6,30]]}},"URL":"https:\/\/doi.org\/10.3339\/ckd.25.012","relation":{},"ISSN":["2384-0242","2384-0250"],"issn-type":[{"type":"print","value":"2384-0242"},{"type":"electronic","value":"2384-0250"}],"subject":[],"published":{"date-parts":[[2025,6,27]]},"assertion":[{"value":"2025-02-27","order":0,"name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2025-05-28","order":1,"name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}},{"value":"2025-06-27","order":2,"name":"published","label":"Published","group":{"name":"publication_history","label":"Publication History"}}]}}