{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,2,10]],"date-time":"2024-02-10T00:43:12Z","timestamp":1707525792250},"reference-count":10,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,2,2]]},"DOI":"10.7759\/cureus.53467","type":"journal-article","created":{"date-parts":[[2024,2,2]],"date-time":"2024-02-02T23:29:13Z","timestamp":1706916553000},"source":"Crossref","is-referenced-by-count":0,"title":["Characteristics of Craniofacial Morphology and Occlusion in Shwachman\u2013Diamond Syndrome: A Case Report of a Japanese Sibling Pair"],"prefix":"10.7759","author":[{"given":"Masahiro","family":"Takahashi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masataka","family":"Ariwa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tetsutaro","family":"Yamaguchi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1038\/ng1062","article-title":"Mutations in SBDS are associated with Shwachman-Diamond syndrome","volume":"33","author":"Boocock GR","year":"2003","unstructured":"Boocock GR, Morrison JA, Popovic M, Richards N, Ellis L, Durie PR, Rommens JM. Mutations in SBDS are associated with Shwachman-Diamond syndrome. Nat Genet. 2003, 33:97-101. 10.1038\/ng1062","journal-title":"Nat Genet"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1749-6632.2011.06349.x","article-title":"Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome","volume":"1242","author":"Dror Y","year":"2011","unstructured":"Dror Y, Donadieu J, Koglmeier J, et al.. Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome. Ann N Y Acad Sci. 2011, 1242:40-55. 10.1111\/j.1749-6632.2011.06349.x","journal-title":"Ann N Y Acad Sci"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1053\/shem.2002.31915","article-title":"Shwachman-Diamond syndrome","volume":"39","author":"Smith OP","year":"2002","unstructured":"Smith OP. Shwachman-Diamond syndrome. Semin Hematol. 2002, 39:95-102. 10.1053\/shem.2002.31915","journal-title":"Semin Hematol"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1016\/s0022-3476(64)80150-5","article-title":"The syndrome of pancreatic insufficiency and bone marrow dysfunction","volume":"65","author":"Shwachman H","year":"1964","unstructured":"Shwachman H, Diamond LK, Oski FA, Khaw KT. The syndrome of pancreatic insufficiency and bone marrow dysfunction. J Pediatr. 1964, 65:645-63. 10.1016\/s0022-3476(64)80150-5","journal-title":"J Pediatr"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1111\/j.1651-2227.1964.tb07237.x","article-title":"Congenital hypoplasia of the exocrine pancreas","volume":"53","author":"BO M","year":"1964","unstructured":"BO M, SH W, LI R. Congenital hypoplasia of the exocrine pancreas. Acta Paediatr (Stockh). 1964, 53:282-93. 10.1111\/j.1651-2227.1964.tb07237.x","journal-title":"Acta Paediatr (Stockh)"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1136\/adc.55.5.331","article-title":"Shwachman's syndrome. A review of 21 cases","volume":"55","author":"Aggett PJ","year":"1980","unstructured":"Aggett PJ, Cavanagh NP, Matthew DJ, Pincott JR, Sutcliffe J, Harries JT. Shwachman's syndrome. A review of 21 cases. Arch Dis Child. 1980, 55:331-47. 10.1136\/adc.55.5.331","journal-title":"Arch Dis Child"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1016\/j.hoc.2018.04.006","article-title":"Diagnosis, treatment, and molecular pathology of Shwachman-Diamond syndrome","volume":"32","author":"Nelson AS","year":"2018","unstructured":"Nelson AS, Myers KC. Diagnosis, treatment, and molecular pathology of Shwachman-Diamond syndrome. Hematol Oncol Clin North Am. 2018, 32:687-700. 10.1016\/j.hoc.2018.04.006","journal-title":"Hematol Oncol Clin North Am"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.2106\/00004623-199402000-00018","article-title":"Orthopaedic features of Shwachman syndrome. A report of two cases","volume":"76","author":"Dhar S","year":"1994","unstructured":"Dhar S, Anderton JM. Orthopaedic features of Shwachman syndrome. A report of two cases. J Bone Joint Surg Am. 1994, 76:278-82. 10.2106\/00004623-199402000-00018","journal-title":"J Bone Joint Surg Am"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1016\/s0016-5085(96)70022-7","article-title":"Shwachman syndrome: exocrine pancreatic dysfunction and variable phenotypic expression","volume":"111","author":"Mack DR","year":"1996","unstructured":"Mack DR, Forstner GG, Wilschanski M, Freedman MH, Durie PR. Shwachman syndrome: exocrine pancreatic dysfunction and variable phenotypic expression. Gastroenterology. 1996, 111:1593-602. 10.1016\/s0016-5085(96)70022-7","journal-title":"Gastroenterology"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.1111\/j.0009-9163.2004.00198.x","article-title":"Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDS","volume":"65","author":"M\u00e4kitie O","year":"2004","unstructured":"M\u00e4kitie O, Ellis L, Durie PR, Morrison JA, Sochett EB, Rommens JM, Cole WG. Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDS. Clin Genet. 2004, 65:101-12. 10.1111\/j.0009-9163.2004.00198.x","journal-title":"Clin Genet"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/226217-characteristics-of-craniofacial-morphology-and-occlusion-in-shwachman-diamond-syndrome-a-case-report-of-a-japanese-sibling-pair","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,9]],"date-time":"2024-02-09T20:14:14Z","timestamp":1707509654000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/226217-characteristics-of-craniofacial-morphology-and-occlusion-in-shwachman-diamond-syndrome-a-case-report-of-a-japanese-sibling-pair"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,2,2]]},"references-count":10,"URL":"https:\/\/doi.org\/10.7759\/cureus.53467","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2024,2,2]]}}}