{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T19:26:50Z","timestamp":1787772410246,"version":"build-2784847793"},"reference-count":5,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"5","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2022,9]]},"abstract":"<jats:sec>\n                    <jats:title\/>\n                    <jats:p>Escobar syndrome (nonlethal type of multiple pterygium syndrome) is a very rare genetic disorder. The central manifestations of Escobar syndrome are the presence of multiple pterygia, fixed joint contractures, and characteristic facies. Here, we report a case of Escobar syndrome with additional features such as monodactyly and hypoplastic pectoralis muscle.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.4103\/jiaps.jiaps_241_21","type":"journal-article","created":{"date-parts":[[2024,5,24]],"date-time":"2024-05-24T10:12:35Z","timestamp":1716545555000},"page":"641-643","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":1,"title":["Escobar syndrome with monodactyly"],"prefix":"10.4103","volume":"27","author":[{"given":"Somnath","family":"Karad","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Imran","family":"Ahmad","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sudhanshu","family":"Tripathi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sheikh Sarfraz","family":"Ali","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R1-29-20240905","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1086\/506257","article-title":"Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal gamma subunit","volume":"79","author":"Hoffmann","year":"2006","journal-title":"Am J Hum Genet"},{"key":"R2-29-20240905","first-page":"47","article-title":"Escobar syndrome affecting two male siblings in a family: A rare case report","volume":"1","author":"Rajput","year":"2013","journal-title":"Scholars J Med Case Rep"},{"key":"R3-29-20240905","doi-asserted-by":"crossref","first-page":"390","DOI":"10.1086\/506256","article-title":"Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndrome","volume":"79","author":"Morgan","year":"2006","journal-title":"Am J Hum Genet"},{"key":"R4-29-20240905","doi-asserted-by":"crossref","first-page":"104","DOI":"10.1016\/S1015-9584(09)60118-4","article-title":"Spectrum of features in pterygium syndrome","volume":"29","author":"Parashar","year":"2006","journal-title":"Asian J Surg"},{"key":"R5-29-20240905","first-page":"609","article-title":"Multiple pterygium syndrome","volume":"132","author":"Escobar","year":"1978","journal-title":"Am J Dis Child"}],"container-title":["Journal of Indian Association of Pediatric Surgeons"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.4103\/jiaps.jiaps_241_21","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T18:44:52Z","timestamp":1787769892000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/jiaps.jiaps_241_21"}},"subtitle":["A rare case report"],"short-title":[],"issued":{"date-parts":[[2022,9]]},"references-count":5,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2022]]}},"URL":"https:\/\/doi.org\/10.4103\/jiaps.jiaps_241_21","relation":{},"ISSN":["0971-9261"],"issn-type":[{"value":"0971-9261","type":"print"}],"subject":[],"published":{"date-parts":[[2022,9]]}}}