{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,5,16]],"date-time":"2024-05-16T04:32:46Z","timestamp":1715833966365},"reference-count":15,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2021,8,24]]},"DOI":"10.7759\/cureus.17403","type":"journal-article","created":{"date-parts":[[2021,8,24]],"date-time":"2021-08-24T09:22:29Z","timestamp":1629796949000},"source":"Crossref","is-referenced-by-count":1,"title":["Management of Knee Flexion Contracture in a Child With 3MC Syndrome Using Taylor Spatial Frame"],"prefix":"10.7759","author":[{"given":"Rayan A","family":"Alloqmani","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mohammed S","family":"Al-Zahrani","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gamal O","family":"Al-Tamimi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Emad A","family":"Bahmead","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mohammed H","family":"Al-Rumaih","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.30878","article-title":"Michels syndrome, Carnevale syndrome, OSA syndrome, and Malpuech syndrome: variable expression of a single disorder (3MC syndrome)?","volume":"137A","author":"Titomanlio L","year":"2005","unstructured":"Titomanlio L, Bennaceur S, Bremond-Gignac D, Baumann C, Dupuy O, Verloes A. Michels syndrome, Carnevale syndrome, OSA syndrome, and Malpuech syndrome: variable expression of a single disorder (3MC syndrome)?. Am J Med Genet A. 2005, 137A:332-5. 10.1002\/ajmg.a.30878","journal-title":"Am J Med Genet A"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320160405","article-title":"A previously undescribed autosomal recessive multiple congenital anomalies\/mental retardation (MCA\/MR) syndrome with growth failure, lip\/palate cleft(s), and urogenital anomalies","volume":"16","author":"Malpuech G","year":"1983","unstructured":"Malpuech G, Demeocq F, Palcoux JB, Vanlieferinghen P. A previously undescribed autosomal recessive multiple congenital anomalies\/mental retardation (MCA\/MR) syndrome with growth failure, lip\/palate cleft(s), and urogenital anomalies. Am J Med Genet. 1983, 16:475-80. 10.1002\/ajmg.1320160405","journal-title":"Am J Med Genet"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320330210","article-title":"Ptosis of eyelids, strabismus, diastasis recti, hip defect, cryptorchidism, and developmental delay in two sibs","volume":"33","author":"Carnevale F","year":"1989","unstructured":"Carnevale F, Krajewska G, Fischetto R, Greco MG, Bonvino A. Ptosis of eyelids, strabismus, diastasis recti, hip defect, cryptorchidism, and developmental delay in two sibs. Am J Med Genet. 1989, 33:186-9. 10.1002\/ajmg.1320330210","journal-title":"Am J Med Genet"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.33.10.884","article-title":"Two sisters with a syndrome of ocular, skeletal, and abdominal abnormalities (OSA syndrome)","volume":"33","author":"Mingarelli R","year":"1996","unstructured":"Mingarelli R, Castriota Scanderbeg A, Dallapiccola B. Two sisters with a syndrome of ocular, skeletal, and abdominal abnormalities (OSA syndrome). J Med Genet. 1996, 33:884-6. 10.1136\/jmg.33.10.884","journal-title":"J Med Genet"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(78)81154-8","article-title":"A clefting syndrome with ocular anterior chamber defect and lid anomalies","volume":"93","author":"Michels VV","year":"1978","unstructured":"Michels VV, Hittner HM, Beaudet AL. A clefting syndrome with ocular anterior chamber defect and lid anomalies. J Pediatr. 1978, 93:444-6. 10.1016\/S0022-3476(78)81154-8","journal-title":"J Pediatr"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1111\/j.0105-2896.2004.0123.x","article-title":"The lectin-complement pathway--its role in innate immunity and evolution","volume":"198","author":"Fujita T","year":"2004","unstructured":"Fujita T, Matsushita M, Endo Y. The lectin-complement pathway--its role in innate immunity and evolution. Immunol Rev. 2004, 198:185-202. 10.1111\/j.0105-2896.2004.0123.x","journal-title":"Immunol Rev"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pgen.1006679","article-title":"COLEC10 is mutated in 3MC patients and regulates early craniofacial development","volume":"13","author":"Munye MM","year":"2017","unstructured":"Munye MM, Diaz-Font A, Ocaka L, et al.. COLEC10 is mutated in 3MC patients and regulates early craniofacial development. PLoS Genet. 2017, 13:e1006679. 10.1371\/journal.pgen.1006679","journal-title":"PLoS Genet"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1097\/01241398-198411000-00009","article-title":"Posterior capsulotomy for the treatment of severe flexion contractures of the knee","volume":"4","author":"Heydarian K","year":"1984","unstructured":"Heydarian K, Akbarnia BA, Jabalameli M, Tabador K. Posterior capsulotomy for the treatment of severe flexion contractures of the knee. J Pediatr Orthop. 1984, 4:700-4. 10.1097\/01241398-198411000-00009","journal-title":"J Pediatr Orthop"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.4103\/2455-3719.190712","article-title":"Gradual correction of knee flexion contracture using external fixation","volume":"2","author":"Vulcano E","year":"2016","unstructured":"Vulcano E, Markowitz J, Fragomen A, Rozbruch SR. Gradual correction of knee flexion contracture using external fixation. J Limb Lengthen Reconstr. 2016, 2:102-7. 10.4103\/2455-3719.190712","journal-title":"J Limb Lengthen Reconstr"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.3390\/ijms21155483","article-title":"Association of polymorphisms of MASP1\/3, COLEC10, and COLEC11 genes with 3MC syndrome","volume":"21","author":"Gajek G","year":"2020","unstructured":"Gajek G, \u015awierzko AS, Cedzy\u0144ski M. Association of polymorphisms of MASP1\/3, COLEC10, and COLEC11 genes with 3MC syndrome. Int J Mol Sci. 2020, 21:5483. 10.3390\/ijms21155483","journal-title":"Int J Mol Sci"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1186\/s13023-015-0345-3","article-title":"Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome","volume":"10","author":"Atik T","year":"2015","unstructured":"Atik T, Koparir A, Bademci G, et al.. Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome. Orphanet J Rare Dis. 2015, 10:128. 10.1186\/s13023-015-0345-3","journal-title":"Orphanet J Rare Dis"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.25000\/acem.505975","article-title":"3MC syndrome: a case report","volume":"4","author":"\u00c7akmakl\u0131 S","year":"2019","unstructured":"\u00c7akmakl\u0131 S, Kandur Y. 3MC syndrome: a case report. Arch Clin Exp Med. 2019, 4:107-9. 10.25000\/acem.505975","journal-title":"Arch Clin Exp Med"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.1597\/15-151","article-title":"Familial recurrence of 3MC syndrome in consanguineous families: a clinical and molecular diagnostic approach with review of the literature","volume":"54","author":"Gardner OK","year":"2017","unstructured":"Gardner OK, Haynes K, Schweitzer D, Johns A, Magee WP, Urata MM, Sanchez-Lara PA. Familial recurrence of 3MC syndrome in consanguineous families: a clinical and molecular diagnostic approach with review of the literature. Cleft Palate Craniofac J. 2017, 54:739-48. 10.1597\/15-151","journal-title":"Cleft Palate Craniofac J"},{"key":"ref14","doi-asserted-by":"publisher","DOI":"10.1097\/01.bpb.0000228380.27239.8a","article-title":"Correction of deformities in children using the Taylor spatial frame","volume":"15","author":"Eidelman M","year":"2006","unstructured":"Eidelman M, Bialik V, Katzman A. Correction of deformities in children using the Taylor spatial frame. J Pediatr Orthop B. 2006, 15:387-95. 10.1097\/01.bpb.0000228380.27239.8a","journal-title":"J Pediatr Orthop B"},{"key":"ref15","doi-asserted-by":"publisher","DOI":"10.1007\/s00402-008-0702-y","article-title":"Distraction osteogenesis for correction of three-dimensional deformities with shortening of lower limbs by Taylor spatial frame","volume":"129","author":"Nakase T","year":"2009","unstructured":"Nakase T, Kitano M, Kawai H, Ueda T, Higuchi C, Hamada M, Yoshikawa H. Distraction osteogenesis for correction of three-dimensional deformities with shortening of lower limbs by Taylor spatial frame. Arch Orthop Trauma Surg. 2009, 129:1197-201. 10.1007\/s00402-008-0702-y","journal-title":"Arch Orthop Trauma Surg"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/66378-management-of-knee-flexion-contracture-in-a-child-with-3mc-syndrome-using-taylor-spatial-frame","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,9]],"date-time":"2024-02-09T19:30:27Z","timestamp":1707507027000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/66378-management-of-knee-flexion-contracture-in-a-child-with-3mc-syndrome-using-taylor-spatial-frame"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,8,24]]},"references-count":15,"URL":"https:\/\/doi.org\/10.7759\/cureus.17403","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2021,8,24]]}}}