{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,7,20]],"date-time":"2025-07-20T03:50:53Z","timestamp":1752983453849,"version":"3.41.0"},"reference-count":14,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2015,9,4]],"date-time":"2015-09-04T00:00:00Z","timestamp":1441324800000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["J Med Case Reports"],"published-print":{"date-parts":[[2015,12]]},"DOI":"10.1186\/s13256-015-0689-2","type":"journal-article","created":{"date-parts":[[2015,9,4]],"date-time":"2015-09-04T16:27:58Z","timestamp":1441384078000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":28,"title":["Neonatal McCune\u2013Albright syndrome with systemic involvement: a case report"],"prefix":"10.1186","volume":"9","author":[{"given":"Rita","family":"Louren\u00e7o","sequence":"first","affiliation":[]},{"given":"Patr\u00edcia","family":"Dias","sequence":"additional","affiliation":[]},{"given":"Raquel","family":"Gouveia","sequence":"additional","affiliation":[]},{"given":"Ana Berta","family":"Sousa","sequence":"additional","affiliation":[]},{"given":"Gra\u00e7a","family":"Oliveira","sequence":"additional","affiliation":[]}],"member":"297","published-online":{"date-parts":[[2015,9,4]]},"reference":[{"key":"689_CR1","doi-asserted-by":"publisher","first-page":"727","DOI":"10.1056\/NEJM193704292161701","volume":"216","author":"F Albright","year":"1937","unstructured":"Albright F, Butler AM, Hampton AO, Smith P. Syndrome characterized by osteitis fibrosa disseminata, areas of pigmentation and endocrine dysfunction with precocious puberty in females. N Eng J Med. 1937;216:727\u201346.","journal-title":"N Eng J Med."},{"key":"689_CR2","doi-asserted-by":"publisher","first-page":"12","DOI":"10.1186\/1750-1172-3-12","volume":"3","author":"CE Dumitrescu","year":"2008","unstructured":"Dumitrescu CE, Collins MT. McCune\u2013Albright syndrome. Orphanet J Rare Dis. 2008;3:12.","journal-title":"Orphanet J Rare Dis."},{"key":"689_CR3","doi-asserted-by":"publisher","first-page":"1688","DOI":"10.1056\/NEJM199112123252403","volume":"325","author":"LS Weinstein","year":"1991","unstructured":"Weinstein LS, Shenker A, Gejman PV, Merino MJ, Friedman E, Spiegel AM. Activating mutations of the stimulatory G protein in the McCune\u2013Albright syndrome. N Engl J Med. 1991;325:1688\u201395.","journal-title":"N Engl J Med."},{"key":"689_CR4","doi-asserted-by":"publisher","first-page":"321","DOI":"10.1111\/j.1399-0004.1986.tb01261.x","volume":"29","author":"R Happle","year":"1986","unstructured":"Happle R. The McCune\u2013Albright syndrome: a lethal gene surviving by mosaicism. Clin Genet. 1986;29:321\u20134.","journal-title":"Clin Genet."},{"key":"689_CR5","doi-asserted-by":"publisher","first-page":"789","DOI":"10.1016\/S0022-3476(99)70302-1","volume":"134","author":"JM Kirk","year":"1999","unstructured":"Kirk JM, Brain CE, Carson DJ, Hyde JC, Grant DB. Cushing\u2019s syndrome caused by nodular adrenal hyperplasia in children with McCune\u2013Albright syndrome. J Pediatr. 1999;134:789\u201392.","journal-title":"J Pediatr."},{"key":"689_CR6","doi-asserted-by":"publisher","first-page":"1508","DOI":"10.1210\/jc.2009-2321","volume":"95","author":"RJ Brown","year":"2010","unstructured":"Brown RJ, Kelly MH, Collins MT. Cushing syndrome in the McCune\u2013Albright syndrome. J Clin Endocrinol Metab. 2010;95:1508\u201315.","journal-title":"J Clin Endocrinol Metab."},{"issue":"Suppl 1","key":"689_CR7","doi-asserted-by":"publisher","first-page":"S4","DOI":"10.1186\/1750-1172-7-S1-S4","volume":"7","author":"MT Collins","year":"2012","unstructured":"Collins MT, Singer FR, Eugster E. McCune\u2013Albright syndrome and the extraskeletal manifestations of fibrous dysplasia. Orphanet J Rare Dis. 2012;7 Suppl 1:S4. Epub 2012 May.","journal-title":"Orphanet J Rare Dis"},{"key":"689_CR8","doi-asserted-by":"crossref","first-page":"641","DOI":"10.1016\/S0026-895X(25)14307-1","volume":"23","author":"WL Combest","year":"1983","unstructured":"Combest WL, Russell DH. Alteration in cyclic AMP-dependent protein kinases and polyamine biosynthetic enzymes during hypertrophy and hyperplasia of the thyroid in the rat. Mol Pharmacol. 1983;23:641\u20137.","journal-title":"Mol Pharmacol."},{"key":"689_CR9","doi-asserted-by":"publisher","first-page":"2383","DOI":"10.1210\/jc.2007-2237","volume":"93","author":"FS Celi","year":"2008","unstructured":"Celi FS, Coppotelli G, Chidakel A, Kelly M, Brillante BA, Shawker T, et al. The role of type 1 and type 2 5'-deiodinase in the pathophysiology of the 3,5,3' triiodothyronine toxicosis of McCune\u2013Albright syndrome. J Clin Endocrinol Metab. 2008;93:2383\u20139.","journal-title":"J Clin Endocrinol Metab."},{"key":"689_CR10","doi-asserted-by":"publisher","first-page":"4413","DOI":"10.1210\/jc.2002-021642","volume":"88","author":"MT Collins","year":"2003","unstructured":"Collins MT, Sarlis NJ, Merino MJ, Monroe J, Crawford SE, Krakoff JA, et al. Thyroid carcinoma in the McCune\u2013Albright syndrome: contributory role of activating Gs alpha mutations. J Clin Endocrinol Metab. 2003;88:4413\u20137.","journal-title":"J Clin Endocrinol Metab."},{"key":"689_CR11","doi-asserted-by":"publisher","first-page":"984","DOI":"10.1111\/j.1651-2227.1991.tb11769.x","volume":"80","author":"M Yoshimoto","year":"1991","unstructured":"Yoshimoto M, Nakayama M, Baba T, Uehara Y, Niikawa N, Ito M, et al. A case of neonatal McCune\u2013Albright syndrome with Cushing syndrome and hyperthyroidism. Acta Paediatr Scand. 1991;80:984\u20137.","journal-title":"Acta Paediatr Scand."},{"issue":"4","key":"689_CR12","doi-asserted-by":"publisher","first-page":"509","DOI":"10.1016\/S0022-3476(05)80943-6","volume":"123","author":"A Shenker","year":"1993","unstructured":"Shenker A, Weinstein LS, Moran A, Pescovitz OH, Charest NJ, Boney CM, et al. Severe endocrine and nonendocrine manifestations of the McCune\u2013Albright syndrome associated with activating mutations of stimulatory G protein GS. J Pediatr. 1993;123(4):509\u201318.","journal-title":"J Pediatr"},{"key":"689_CR13","doi-asserted-by":"publisher","first-page":"504","DOI":"10.1046\/j.1525-1470.2001.1862003.x","volume":"18","author":"JH Davies","year":"2001","unstructured":"Davies JH, Barton JS, Gregory JW, Mills C. Infantile McCune\u2013Albright syndrome. Pediatr Dermatol. 2001;18:504\u20136.","journal-title":"Pediatr Dermatol."},{"key":"689_CR14","doi-asserted-by":"publisher","first-page":"154","DOI":"10.1016\/S0168-8278(00)80202-0","volume":"32","author":"ES Silva","year":"2000","unstructured":"Silva ES, Lumbroso S, Medina M, Gillerot Y, Sultan C, Sokal EM. Demonstration of McCune\u2013Albright mutations in the liver of children with high gammaGT progressive cholestasis. J Hepatol. 2000;32:154\u20138.","journal-title":"J Hepatol."}],"container-title":["Journal of Medical Case Reports"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1186\/s13256-015-0689-2.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1186\/s13256-015-0689-2\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1186\/s13256-015-0689-2.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,5,30]],"date-time":"2025-05-30T12:39:18Z","timestamp":1748608758000},"score":1,"resource":{"primary":{"URL":"http:\/\/jmedicalcasereports.biomedcentral.com\/articles\/10.1186\/s13256-015-0689-2"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,9,4]]},"references-count":14,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2015,12]]}},"alternative-id":["689"],"URL":"https:\/\/doi.org\/10.1186\/s13256-015-0689-2","relation":{},"ISSN":["1752-1947"],"issn-type":[{"type":"electronic","value":"1752-1947"}],"subject":[],"published":{"date-parts":[[2015,9,4]]},"article-number":"189"}}