{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,2]],"date-time":"2026-05-02T13:08:06Z","timestamp":1777727286489,"version":"3.51.4"},"reference-count":18,"publisher":"SAGE Publications","issue":"4","license":[{"start":{"date-parts":[[2026,4,1]],"date-time":"2026-04-01T00:00:00Z","timestamp":1775001600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"},{"start":{"date-parts":[[2026,4,1]],"date-time":"2026-04-01T00:00:00Z","timestamp":1775001600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"funder":[{"name":"Scientific Research Project of Chengdu Medical Association","award":["No:2024155"],"award-info":[{"award-number":["No:2024155"]}]},{"name":"the High-level Talent Introduction Project of the First Affiliated Hospital of Chengdu Medical College","award":["CYFY-GQ64"],"award-info":[{"award-number":["CYFY-GQ64"]}]},{"name":"the High-level Talent Introduction Project of the First Affiliated Hospital of Chengdu Medical College","award":["CYFY-GQ69"],"award-info":[{"award-number":["CYFY-GQ69"]}]}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["J Int Med Res"],"published-print":{"date-parts":[[2026,4]]},"abstract":"<jats:p>\n                    Pseudohypoparathyroidism is a rare genetic disorder characterized by hypocalcemia, hyperphosphatemia, and elevated serum intact parathyroid hormone levels. The taxonomy of pseudohypoparathyroidism is intricate, with heterogeneous clinical presentations and lack of specificity. A school-age Chinese girl was admitted with a 2-day history of fever and a single episode of seizure, with no clinical features of Albright hereditary osteodystrophy. Physical examination revealed positive Chvostek\u2019s and Trousseau\u2019s signs, with no other significant abnormalities. Laboratory tests revealed hypocalcemia, elevated intact parathyroid hormone levels, and transient hypokalemia (2.8\u2009mmol\/L). Whole-exome sequencing showed a 2.1-Kb deletion of exons 4\u20136 in syntaxin 16 (\n                    <jats:italic toggle=\"yes\">STX16<\/jats:italic>\n                    ); however, her parents did not exhibit any such alterations. The patient was finally diagnosed with pseudohypoparathyroidism and administered calcium gluconate perfusion, calcitriol, and elemental calcium. After discharge, her calcitriol and elemental calcium dosages were gradually tapered in the outpatient setting. By the 1-year follow-up, hypocalcemia had been largely corrected; however, her intact parathyroid hormone level remained above the normal reference range. This case of sporadic pseudohypoparathyroidism type Ib with a 2.1-Kb\n                    <jats:italic toggle=\"yes\">STX16<\/jats:italic>\n                    deletion underscores that pseudohypoparathyroidism can present as fever-induced seizure with transient hypokalemia, highlighting the importance of metabolic and genetic screening in children who experience seizures.\n                  <\/jats:p>","DOI":"10.1177\/03000605261438919","type":"journal-article","created":{"date-parts":[[2026,4,13]],"date-time":"2026-04-13T02:18:49Z","timestamp":1776046729000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["Pseudohypoparathyroidism in a Chinese girl: A case report"],"prefix":"10.1177","volume":"54","author":[{"given":"Xue-Mei","family":"Zhao","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Xindu District People\u2019s Hospital, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jing-Rong","family":"Yang","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Xindu District People\u2019s Hospital, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Huan","family":"Yin","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, the First Affiliated Hospital of Chengdu Medical College, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chang-Qiang","family":"Yang","sequence":"additional","affiliation":[{"name":"Department of Cardiology, the First Affiliated Hospital of Chengdu Medical College, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4679-0330","authenticated-orcid":false,"given":"Yue","family":"Song","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, the First Affiliated Hospital of Chengdu Medical College, China"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2026,4,12]]},"reference":[{"key":"e_1_3_8_2_2","doi-asserted-by":"publisher","DOI":"10.1111\/cen.13516"},{"key":"e_1_3_8_3_2","doi-asserted-by":"publisher","DOI":"10.1007\/s12020-022-03204-7"},{"key":"e_1_3_8_4_2","doi-asserted-by":"publisher","DOI":"10.1097\/MOP.0000000000000783"},{"key":"e_1_3_8_5_2","doi-asserted-by":"publisher","DOI":"10.1210\/jc.2012-2920"},{"key":"e_1_3_8_6_2","doi-asserted-by":"publisher","DOI":"10.1530\/EJE-16-0107"},{"key":"e_1_3_8_7_2","doi-asserted-by":"publisher","DOI":"10.1210\/jc.2015-4310"},{"key":"e_1_3_8_8_2","doi-asserted-by":"publisher","DOI":"10.1515\/jpem-2023-0562"},{"key":"e_1_3_8_9_2","doi-asserted-by":"publisher","DOI":"10.1111\/head.12246"},{"key":"e_1_3_8_10_2","doi-asserted-by":"publisher","DOI":"10.1111\/epi.14016"},{"key":"e_1_3_8_11_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.seizure.2025.07.002"},{"key":"e_1_3_8_12_2","doi-asserted-by":"publisher","DOI":"10.1097\/RHU.0000000000002265"},{"key":"e_1_3_8_13_2","doi-asserted-by":"publisher","DOI":"10.1186\/s12902-022-01011-9"},{"key":"e_1_3_8_14_2","doi-asserted-by":"publisher","DOI":"10.3389\/fendo.2020.00539"},{"key":"e_1_3_8_15_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.ando.2022.09.022"},{"key":"e_1_3_8_16_2","doi-asserted-by":"publisher","DOI":"10.1210\/jc.2007-0869"},{"key":"e_1_3_8_17_2","first-page":"112","article-title":"An intricate case of sporadic pseudohypoparathyroidism type 1B with a review of literature","volume":"65","author":"Ramalho E Silva JD","year":"2021","unstructured":"Ramalho E Silva JD, Da Rocha GFMA, Oliveira MJM. An intricate case of sporadic pseudohypoparathyroidism type 1B with a review of literature. Arch Endocrinol Metab 2021; 65: 112\u2013116.","journal-title":"Arch Endocrinol Metab"},{"key":"e_1_3_8_18_2","doi-asserted-by":"publisher","DOI":"10.1210\/clinem\/dgab660"},{"key":"e_1_3_8_19_2","doi-asserted-by":"publisher","DOI":"10.1172\/JCI167953"}],"container-title":["Journal of International Medical Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/03000605261438919","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/full-xml\/10.1177\/03000605261438919","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/03000605261438919","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,29]],"date-time":"2026-04-29T10:49:04Z","timestamp":1777459744000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.sagepub.com\/doi\/10.1177\/03000605261438919"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,4]]},"references-count":18,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2026,4]]}},"alternative-id":["10.1177\/03000605261438919"],"URL":"https:\/\/doi.org\/10.1177\/03000605261438919","relation":{},"ISSN":["0300-0605","1473-2300"],"issn-type":[{"value":"0300-0605","type":"print"},{"value":"1473-2300","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,4]]},"article-number":"03000605261438919"}}