{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,29]],"date-time":"2026-07-29T23:07:37Z","timestamp":1785366457551,"version":"3.55.0"},"reference-count":13,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2005,5,11]],"date-time":"2005-05-11T00:00:00Z","timestamp":1115769600000},"content-version":"vor","delay-in-days":10,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Oral Diseases"],"published-print":{"date-parts":[[2005,5]]},"abstract":"<jats:p>The trismus\u2010pseudocamptodactyly syndrome (TPS) is a rare condition inherited as an autosomal dominant trait with variable expressivity. Clinically the syndrome is characterized by decreased ability to open the mouth and curvature of the fingers at the level of interphalangic joints while attempting dorsiflexion of the wrist (pseudocamptodactyly). A 6\u2010year\u2010old male patient from Guatemala with this syndrome is presented. The surgical treatment consisted of bilateral coronoid amputation to resolve the pseudotrismus. The procedure was successful and the patient achieved normal function.<\/jats:p>","DOI":"10.1111\/j.1601-0825.2005.01005.x","type":"journal-article","created":{"date-parts":[[2010,8,2]],"date-time":"2010-08-02T21:58:33Z","timestamp":1280786313000},"page":"186-189","source":"Crossref","is-referenced-by-count":26,"title":["Trismus\u2010pseudocamptodactyly syndrome (Hecht\u2013Beals\u2019 syndrome): case report and literature review"],"prefix":"10.1111","volume":"11","author":[{"given":"R","family":"Carlos","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E","family":"Contreras","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J","family":"Cabrera","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,5,11]]},"reference":[{"key":"e_1_2_5_2_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00326944"},{"key":"e_1_2_5_3_1","doi-asserted-by":"crossref","DOI":"10.1093\/oso\/9780195118612.001.0001","volume-title":"Syndromes of the head and neck","author":"Gorlin RJ","year":"2001"},{"key":"e_1_2_5_4_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320110208"},{"key":"e_1_2_5_5_1","first-page":"96","article-title":"Inability to open the mouth fully: an autosomal dominant phenotype with facultative camptodactyly and short stature","author":"Hecht F","year":"1969","journal-title":"Birth Defects Orig Art Ser"},{"key":"e_1_2_5_6_1","doi-asserted-by":"publisher","DOI":"10.1097\/01.SAP.0000046787.17899.83"},{"key":"e_1_2_5_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(74)80453-1"},{"key":"e_1_2_5_8_1","volume-title":"Online Mendelian Inheritance in Man, OMIM (TM)"},{"key":"e_1_2_5_9_1","first-page":"33","article-title":"Trismus\u2010pseudocamptodactyly: a case report","volume":"4","author":"Pelo S","year":"2003","journal-title":"Eur J Paediatr Dent"},{"key":"e_1_2_5_10_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320120116"},{"key":"e_1_2_5_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0753-9053(05)80481-8"},{"key":"e_1_2_5_12_1","first-page":"144","article-title":"Trismus\u2010pseudocamptodctyly syndrome: report of one case","volume":"35","author":"Teng RJ","year":"1994","journal-title":"Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi"},{"key":"e_1_2_5_13_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1985.tb00394.x"},{"key":"e_1_2_5_14_1","first-page":"99","article-title":"Autosomal dominant inheritance of shortening of the flexor profundus muscle\u2010tendon unit with limitation of jaw excursion","author":"Wilson RV","year":"1969","journal-title":"Birth Defects"}],"container-title":["Oral Diseases"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fj.1601-0825.2005.01005.x","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/j.1601-0825.2005.01005.x","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,3,28]],"date-time":"2024-03-28T23:55:17Z","timestamp":1711670117000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/j.1601-0825.2005.01005.x"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2005,5]]},"references-count":13,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2005,5]]}},"alternative-id":["10.1111\/j.1601-0825.2005.01005.x"],"URL":"https:\/\/doi.org\/10.1111\/j.1601-0825.2005.01005.x","archive":["Portico"],"relation":{},"ISSN":["1354-523X","1601-0825"],"issn-type":[{"value":"1354-523X","type":"print"},{"value":"1601-0825","type":"electronic"}],"subject":[],"published":{"date-parts":[[2005,5]]}}}