{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,3]],"date-time":"2026-06-03T11:57:43Z","timestamp":1780487863923,"version":"3.54.1"},"reference-count":56,"publisher":"Walter de Gruyter GmbH","issue":"1-2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2015,1,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Periodic paralysis associated with hyperthyroidism and hypokalemia is an uncommon disorder reported primarily in Asian males and rarely in children. We report three Hispanic adolescent males who were seen with Graves\u2019 disease (GD) and THPP.<\/jats:p><jats:p>The method used was chart review.<\/jats:p><jats:p>Two of these boys presented with episodes of paralysis and were diagnosed with GD. The third was initially seen with hyperthyroidism and developed weakness and paralysis when his disease progressed because of therapeutic noncompliance. Hypokalemia was documented in two of the three patients with the third not seen during paralysis. Intravenous K<\/jats:p><jats:p>THPP is considered uncommon except in Asian males and rare in childhood and adolescence. Its occurrence in these three Hispanic boys suggests that it may occur more frequently in the young and in the USA than has been suspected, especially with the changing national demographics. We believe that our experience should raise the awareness of THPP among pediatric care providers.<\/jats:p>","DOI":"10.1515\/jpem-2014-0016","type":"journal-article","created":{"date-parts":[[2014,8,12]],"date-time":"2014-08-12T08:07:02Z","timestamp":1407830822000},"source":"Crossref","is-referenced-by-count":5,"title":["Thyrotoxic, hypokalemic periodic paralysis (THPP) in adolescents"],"prefix":"10.1515","volume":"28","author":[{"given":"Hiba","family":"Al-Zubeidi","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carla","family":"Demeterco","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kenneth Lee","family":"Jones","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"374","reference":[{"key":"ref291","doi-asserted-by":"crossref","first-page":"427","DOI":"10.4158\/EP.12.4.427","article-title":"Thyrotoxic periodic paralysis in a Hispanic man after the administration of prednisone","volume":"12","author":"Liu","year":"2006","journal-title":"Endocr Pract"},{"key":"ref351","first-page":"383","article-title":"Thyrotoxic hypokalaemic periodic paralysis in a Hispanic male","author":"Zumo LA","year":"2002","journal-title":"J Natl Med Assoc"},{"key":"ref361","first-page":"659","article-title":"hypokalaemic paralysis in a Black man","author":"Salifu","year":"2001","journal-title":"J Med"},{"key":"ref331","first-page":"1","article-title":"Periodic paralysis complicating thyrotoxicosis in Chinese","author":"McFadzean","year":"1967","journal-title":"Young Med"},{"key":"ref471","first-page":"234","article-title":"Hypokalemic periodic paralysis : an autosomal dominant muscle disorder caused by mutations in a voltage - 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