{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,14]],"date-time":"2026-08-14T19:54:12Z","timestamp":1786737252667,"version":"build-2736575974"},"reference-count":14,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Family Med Prim Care"],"published-print":{"date-parts":[[2020]]},"DOI":"10.4103\/jfmpc.jfmpc_237_20","type":"journal-article","created":{"date-parts":[[2020,6,1]],"date-time":"2020-06-01T12:03:53Z","timestamp":1591013033000},"page":"2531","source":"Crossref","is-referenced-by-count":11,"title":["Triple A syndrome (Allgrove syndrome) \u2013 A journey from clinical symptoms to a syndrome"],"prefix":"10.4103","volume":"9","author":[{"given":"Deepak","family":"Kumar","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Prakarti","family":"Yadav","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"GopalK","family":"Bohra","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"MahendraK","family":"Garg","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"key-10.4103\/2249-4863.285100-1","doi-asserted-by":"crossref","first-page":"1284","DOI":"10.1016\/S0140-6736(78)91268-0","article-title":"Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production","author":"Allgrove","year":"1978","journal-title":"Lancet"},{"key":"key-10.4103\/2249-4863.285100-2","first-page":"277","article-title":"ACTH resistance syndromes","author":"Huebner","year":"1999","journal-title":"J Pediatr Endocrinol Metab"},{"key":"key-10.4103\/2249-4863.285100-3","first-page":"1512","article-title":"AAA syndrome, case report of a rare disease","author":"Shah","year":"2017","journal-title":"Pak J Med Sci"},{"key":"key-10.4103\/2249-4863.285100-4","doi-asserted-by":"crossref","first-page":"799","DOI":"10.1515\/jpem-2018-0023","article-title":"Clinical heterogeneity and molecular profile of triple A syndrome: A study of seven cases","author":"Singh","year":"2018","journal-title":"J Pediatr Endocrinol Metab"},{"key":"key-10.4103\/2249-4863.285100-5","first-page":"790","article-title":"Allgrove syndrome: Adrenal insufficiency with hypertensive encephalopathy","author":"Aftab","year":"2016","journal-title":"J Coll Physicians Surg Pak"},{"key":"key-10.4103\/2249-4863.285100-6","doi-asserted-by":"crossref","first-page":"604","DOI":"10.3803\/EnM.2015.30.4.604","article-title":"Allgrove (Triple A) syndrome: A case report from the Kashmir Valley","author":"Misgar","year":"2015","journal-title":"Endocrinol Metab"},{"key":"key-10.4103\/2249-4863.285100-7","doi-asserted-by":"crossref","first-page":"18","DOI":"10.1007\/BF01972967","article-title":"The \u201c4A\u201d syndrome: Adrenocortical insufficiency associated with achalasia, alacrima, autonomic and other neurological abnormalities","author":"Gazarian","year":"1995","journal-title":"Eur J Pediatr"},{"key":"key-10.4103\/2249-4863.285100-8","doi-asserted-by":"crossref","first-page":"415","DOI":"10.1034\/j.1399-0004.2003.00070.x","article-title":"Triple A syndrome: Genotype-phenotype assessment","author":"Prpic","year":"2003","journal-title":"Clin Genet"},{"key":"key-10.4103\/2249-4863.285100-9","doi-asserted-by":"crossref","first-page":"37","DOI":"10.4103\/2230-8229.97016","article-title":"Allgrove's syndrome: Case report and literature review","author":"Yasawy","year":"2009","journal-title":"J Family Community Med"},{"key":"key-10.4103\/2249-4863.285100-10","doi-asserted-by":"crossref","first-page":"779","DOI":"10.1136\/adc.68.6.779","article-title":"Neurological and adrenal dysfunction in the adrenal insufficiency\/alacrima\/achalasia (3A) syndrome","author":"Grant","year":"1993","journal-title":"Arch Dis Child"},{"key":"key-10.4103\/2249-4863.285100-11","doi-asserted-by":"crossref","first-page":"667","DOI":"10.1097\/00000478-200305000-00010","article-title":"Achalasia of the cardia in Allgrove's (triple A) syndrome: Histopathologic study of 10 cases","author":"Khelif","year":"2003","journal-title":"Am J Surg Pathol"},{"key":"key-10.4103\/2249-4863.285100-12","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1007\/s42000-018-0089-2","article-title":"Triple A syndrome: Two siblings with a novel mutation in the AAAS gene","author":"Bouliari","year":"2019","journal-title":"Hormones (Athens)"},{"key":"key-10.4103\/2249-4863.285100-13","doi-asserted-by":"crossref","first-page":"2061","DOI":"10.1093\/hmg\/5.12.2061","article-title":"Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster","author":"Weber","year":"1996","journal-title":"Hum Mol Genet"},{"key":"key-10.4103\/2249-4863.285100-14","doi-asserted-by":"crossref","first-page":"363","DOI":"10.1007\/s00431-017-3068-8","article-title":"Clinical and genetic characterisation of a series of patients with triple A syndrome","author":"Kurnaz","year":"2018","journal-title":"Eur J Pediatr"}],"container-title":["Journal of Family Medicine and Primary Care"],"original-title":[],"language":"en","deposited":{"date-parts":[[2026,8,14]],"date-time":"2026-08-14T18:52:08Z","timestamp":1786733528000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/jfmpc.jfmpc_237_20"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020]]},"references-count":14,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2020]]}},"alternative-id":["285100"],"URL":"https:\/\/doi.org\/10.4103\/jfmpc.jfmpc_237_20","relation":{},"ISSN":["2249-4863"],"issn-type":[{"value":"2249-4863","type":"print"}],"subject":[],"published":{"date-parts":[[2020]]}}}