{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,12]],"date-time":"2026-01-12T23:59:22Z","timestamp":1768262362581,"version":"3.49.0"},"reference-count":14,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2021,11,6]]},"DOI":"10.7759\/cureus.19316","type":"journal-article","created":{"date-parts":[[2021,11,6]],"date-time":"2021-11-06T21:02:37Z","timestamp":1636232557000},"source":"Crossref","is-referenced-by-count":6,"title":["Mineralocorticoid Deficiency as an Early Presenting Symptom of Allgrove Syndrome With Novel Mutation: A Case Report"],"prefix":"10.7759","author":[{"given":"Hashem A","family":"AlOmran","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fadi","family":"Busaleh","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zahra","family":"Alhashim","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Manal","family":"AlHelal","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yasen","family":"Alsaleh","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aida","family":"AlJabri","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zahra A","family":"AlGhadeer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fatimah  Y","family":"AlHejji","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mousa","family":"AlMazeedi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Abdulelah M","family":"Al dandan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(78)91268-0","article-title":"Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production","volume":"311","author":"Allgrove JG","year":"1978","unstructured":"Allgrove JG, Clayden GS, Grant DB, Macaulay JC. Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production. Lancet. 1978, 311:1284-6. 10.1016\/S0140-6736(78)91268-0","journal-title":"Lancet"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1097","article-title":"Case report of a familial triple: a syndrome and review of the literature","volume":"99","author":"Gaiani F","year":"2020","unstructured":"Gaiani F, Gismondi P, Minelli R, et al.. Case report of a familial triple: a syndrome and review of the literature. Medicine (Baltimore). 2020, 99:e20474. 10.1097","journal-title":"Medicine (Baltimore)"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.4103\/jfmpc.jfmpc_237_20","article-title":"Triple A syndrome (Allgrove syndrome)-A journey from clinical symptoms to a syndrome","volume":"9","author":"Yadav P","year":"2020","unstructured":"Yadav P, Kumar D, Bohra GK, Garg MK. Triple A syndrome (Allgrove syndrome)-A journey from clinical symptoms to a syndrome. J Family Med Prim Care. 2020, 9:2531-4. 10.4103\/jfmpc.jfmpc_237_20","journal-title":"J Family Med Prim Care"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.12659\/ajcr.899546","article-title":"Alacrima as a harbinger of adrenal insufficiency in a child with Allgrove syndrome","volume":"17","author":"Brown B","year":"2016","unstructured":"Brown B, Agdere L, Muntean C, David K. Alacrima as a harbinger of adrenal insufficiency in a child with Allgrove syndrome. Am J Case Rep. 2016, 17:703-6. 10.12659\/ajcr.899546","journal-title":"Am J Case Rep"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.4103\/jdep.jdep_11_18","article-title":"Allgrove syndrome (Triple-A Syndrome): a case report from north India","volume":"2","author":"Ashraf H","year":"2019","unstructured":"Ashraf H, Varshney N, Juned MD, Siddiqui SS. Allgrove syndrome (Triple-A Syndrome): a case report from north India. J Diabetes Endocr Pract. 2019, 2:13-5. 10.4103\/jdep.jdep_11_18","journal-title":"J Diabetes Endocr Pract"},{"key":"ref6","article-title":"Allgrove syndrome","volume":"53","author":"Kilicli F","year":"20121","unstructured":"Kilicli F, Acibucu F, Senel S, Dokmetas HS. Allgrove syndrome. Singapore Med J. 20121, 53:92-4.","journal-title":"Singapore Med J"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.2147\/PHMT.S173081","article-title":"Triple A syndrome (Allgrove syndrome): improving outcomes with a multidisciplinary approach","volume":"10","author":"Flokas ME","year":"2019","unstructured":"Flokas ME, Tomani M, Agdere L, Brown B. Triple A syndrome (Allgrove syndrome): improving outcomes with a multidisciplinary approach. Pediatric Health Med Ther. 2019, 10:99-106. 10.2147\/PHMT.S173081","journal-title":"Pediatric Health Med Ther"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.12669\/pjms.336.13684","article-title":"AAA syndrome, case report of a rare disease","volume":"33","author":"Et al","year":"2017","unstructured":"Et al, Shah SW. AAA syndrome, case report of a rare disease. Pak J Med Sci. 2017, 33:1512-16. 10.12669\/pjms.336.13684","journal-title":"Pak J Med Sci"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1177\/0049475520961944","article-title":"Triple A syndrome: a case report","volume":"51","author":"Manoria P","year":"2021","unstructured":"Manoria P. Triple A syndrome: a case report. Trop Doct. 2021, 51:263-5. 10.1177\/0049475520961944","journal-title":"Trop Doct"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.1530\/EJE-17-0642","article-title":"Triple-A syndrome: a wide spectrum of adrenal dysfunction","volume":"178","author":"Roucher-Boulez F","year":"20181","unstructured":"Roucher-Boulez F, de la Perriere AB, Jacquez A, et al.. Triple-A syndrome: a wide spectrum of adrenal dysfunction. Eur J Endocrinol. 20181, 178:199-207. 10.1530\/EJE-17-0642","journal-title":"Eur J Endocrinol"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.18700\/jnc.170035","article-title":"Pharmacologic characteristics of corticosteroids","volume":"10","author":"Samuel S","year":"2017","unstructured":"Samuel S, Nguyen T, Choi A. Pharmacologic characteristics of corticosteroids. J Neurocrit Care. 2017, 10:53-9. 10.18700\/jnc.170035","journal-title":"J Neurocrit Care"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1016\/j.beem.2008.10.014","article-title":"Genetics of congenital adrenal hyperplasia","volume":"23","author":"Krone N","year":"2009","unstructured":"Krone N, Arlt W. Genetics of congenital adrenal hyperplasia. Best Pract Res Clin Endocrinol Metab. 2009, 23:181-92. 10.1016\/j.beem.2008.10.014","journal-title":"Best Pract Res Clin Endocrinol Metab"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.5144\/0256-4947.2000.279","article-title":"Achalasia-Alacrima-Acth insentivity syndrome (Triple A syndrome) in a Saudi Family","volume":"20","author":"Modebe O","year":"2000","unstructured":"Modebe O. Achalasia-Alacrima-Acth insentivity syndrome (Triple A syndrome) in a Saudi Family. Ann Saudi Med. 2000, 20:279-82. 10.5144\/0256-4947.2000.279","journal-title":"Ann Saudi Med"},{"key":"ref14","doi-asserted-by":"publisher","DOI":"10.9734\/bpi\/nfmmr\/v10\/11994D","article-title":"Study on primary adrenal insufficiency (PAI): experience in a major teaching hospital, Riyadh, Saudi Arabia","volume":"10","author":"Al-Jurayyan NA","year":"2021","unstructured":"Al-Jurayyan NA. Study on primary adrenal insufficiency (PAI): experience in a major teaching hospital, Riyadh, Saudi Arabia. New Front Med Med Res. 2021, 10:56-61. 10.9734\/bpi\/nfmmr\/v10\/11994D","journal-title":"New Front Med Med Res"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/74593-mineralocorticoid-deficiency-as-an-early-presenting-symptom-of-allgrove-syndrome-with-novel-mutation-a-case-report","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,9]],"date-time":"2024-02-09T19:33:05Z","timestamp":1707507185000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/74593-mineralocorticoid-deficiency-as-an-early-presenting-symptom-of-allgrove-syndrome-with-novel-mutation-a-case-report"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,11,6]]},"references-count":14,"URL":"https:\/\/doi.org\/10.7759\/cureus.19316","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2021,11,6]]}}}