{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,19]],"date-time":"2026-10-19T15:56:48Z","timestamp":1792425408053,"version":"4.5.0"},"reference-count":31,"publisher":"Springer Science and Business Media LLC","issue":"5","license":[{"start":{"date-parts":[[2022,12,13]],"date-time":"2022-12-13T00:00:00Z","timestamp":1670889600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"},{"start":{"date-parts":[[2022,12,13]],"date-time":"2022-12-13T00:00:00Z","timestamp":1670889600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Childs Nerv Syst"],"published-print":{"date-parts":[[2023,5]]},"DOI":"10.1007\/s00381-022-05788-x","type":"journal-article","created":{"date-parts":[[2022,12,13]],"date-time":"2022-12-13T15:03:55Z","timestamp":1670943835000},"page":"1317-1322","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Multisuture craniosynostosis: a case report of unusual presentation of chromosome 14q32 deletion"],"prefix":"10.1007","volume":"39","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6040-0784","authenticated-orcid":false,"given":"Sarut","family":"Chaisrisawadisuk","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3224-8070","authenticated-orcid":false,"given":"Nithiwat","family":"Vatanavicharn","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3931-937X","authenticated-orcid":false,"given":"Inthira","family":"Khampalikit","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2136-0315","authenticated-orcid":false,"given":"Mark H.","family":"Moore","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2022,12,13]]},"reference":[{"issue":"3","key":"5788_CR1","doi-asserted-by":"publisher","first-page":"370","DOI":"10.3171\/jns.1982.57.3.0370","volume":"57","author":"D Renier","year":"1982","unstructured":"Renier D, Sainte-Rose C, Marchac D, Hirsch JF (1982) Intracranial pressure in craniostenosis. J Neurosurg 57(3):370\u2013377. https:\/\/doi.org\/10.3171\/jns.1982.57.3.0370","journal-title":"J Neurosurg"},{"issue":"5","key":"5788_CR2","doi-asserted-by":"publisher","first-page":"269","DOI":"10.1007\/BF00301758","volume":"11","author":"DN Thompson","year":"1995","unstructured":"Thompson DN, Harkness W, Jones B, Gonsalez S, Andar U, Hayward R (1995) Subdural intracranial pressure monitoring in craniosynostosis: its role in surgical management. Childs Nerv Syst 11(5):269\u2013275. https:\/\/doi.org\/10.1007\/BF00301758","journal-title":"Childs Nerv Syst"},{"issue":"10","key":"5788_CR3","doi-asserted-by":"publisher","first-page":"913","DOI":"10.1007\/s00381-004-1117-x","volume":"21","author":"G Tamburrini","year":"2005","unstructured":"Tamburrini G, Caldarelli M, Massimi L, Santini P, Di Rocco C (2005) Intracranial pressure monitoring in children with single suture and complex craniosynostosis: a review. Childs Nerv Syst 21(10):913\u2013921. https:\/\/doi.org\/10.1007\/s00381-004-1117-x","journal-title":"Childs Nerv Syst"},{"key":"5788_CR4","doi-asserted-by":"publisher","unstructured":"Judy BF, Swanson JW, Yang W, Storm PB, Bartlett SP, Taylor JA, Heuer GG et al (2018) Intraoperative intracranial pressure monitoring in the pediatric craniosynostosis population. J Neurosurg Pediatr 22(5):475\u2013480. https:\/\/doi.org\/10.3171\/2018.5.PEDS1876","DOI":"10.3171\/2018.5.PEDS1876"},{"issue":"6","key":"5788_CR5","doi-asserted-by":"publisher","first-page":"1735","DOI":"10.1097\/SCS.0000000000002016","volume":"26","author":"IM Mathijssen","year":"2015","unstructured":"Mathijssen IM (2015) Guideline for care of patients with the diagnoses of craniosynostosis: working group on craniosynostosis. J Craniofac Surg 26(6):1735\u20131807. https:\/\/doi.org\/10.1097\/SCS.0000000000002016","journal-title":"J Craniofac Surg"},{"issue":"5","key":"5788_CR6","doi-asserted-by":"publisher","first-page":"1087","DOI":"10.1016\/j.bjps.2020.10.049","volume":"74","author":"IMJ Mathijssen","year":"2021","unstructured":"Mathijssen IMJ, Wolvius EB, Spoor JKH, van Veelen MC, Versnel SL (2021) Secondary vault reconstruction after open or minimal invasive correction for unisutural, multisutural or syndromic craniosynostosis: a cohort study on the impact of diagnosis and type of initial surgical technique. J Plast Reconstr Aesthet Surg 74(5):1087\u20131092. https:\/\/doi.org\/10.1016\/j.bjps.2020.10.049","journal-title":"J Plast Reconstr Aesthet Surg"},{"issue":"6","key":"5788_CR7","doi-asserted-by":"publisher","first-page":"1209e","DOI":"10.1097\/PRS.0000000000009046","volume":"149","author":"AS Xue","year":"2022","unstructured":"Xue AS, Buchanan EP, Hollier LH Jr (2022) Update in management of craniosynostosis. Plast Reconstr Surg 149(6):1209e\u20131223e. https:\/\/doi.org\/10.1097\/PRS.0000000000009046","journal-title":"Plast Reconstr Surg"},{"issue":"2","key":"5788_CR8","doi-asserted-by":"publisher","first-page":"141","DOI":"10.1016\/j.cps.2018.11.009","volume":"46","author":"R Sawh-Martinez","year":"2019","unstructured":"Sawh-Martinez R, Steinbacher DM (2019) Syndromic craniosynostosis. Clin Plast Surg 46(2):141\u2013155. https:\/\/doi.org\/10.1016\/j.cps.2018.11.009","journal-title":"Clin Plast Surg"},{"issue":"6","key":"5788_CR9","doi-asserted-by":"publisher","first-page":"622","DOI":"10.1097\/MOP.0000000000000542","volume":"29","author":"AOM Wilkie","year":"2017","unstructured":"Wilkie AOM, Johnson D, Wall SA (2017) Clinical genetics of craniosynostosis. Curr Opin Pediatr 29(6):622\u2013628. https:\/\/doi.org\/10.1097\/MOP.0000000000000542","journal-title":"Curr Opin Pediatr"},{"issue":"1","key":"5788_CR10","doi-asserted-by":"publisher","first-page":"282","DOI":"10.1097\/SCS.0000000000007072","volume":"32","author":"S Chaisrisawadisuk","year":"2021","unstructured":"Chaisrisawadisuk S, Anderson PJ, Moore MH (2021) Neo-sagittal suture formation after cranial vault remodeling in sagittal craniosynostosis. J Craniofac Surg 32(1):282\u2013284. https:\/\/doi.org\/10.1097\/SCS.0000000000007072","journal-title":"J Craniofac Surg"},{"issue":"8","key":"5788_CR11","doi-asserted-by":"publisher","first-page":"2651","DOI":"10.1097\/SCS.0000000000007886","volume":"32","author":"MH Moore","year":"2021","unstructured":"Moore MH, Chaisrisawadisuk S, Prasad V, Santoreneos S, Molloy CJ (2021) Secondary raised intracranial pressure after cranial vault remodeling for isolated sagittal craniosynostosis. J Craniofac Surg 32(8):2651\u20132655. https:\/\/doi.org\/10.1097\/SCS.0000000000007886","journal-title":"J Craniofac Surg"},{"key":"5788_CR12","doi-asserted-by":"publisher","unstructured":"Chaisrisawadisuk S, Hammam E, Molloy CJ, Barnett C, Anderson PJ, Moore MH (2021) Severe cloverleaf skull deformity in c.1061C>G (p.Ser354Cys) mutated fibroblast growth factor receptor 2 gene in Crouzon syndrome. J Craniofac Surg 32(1):261\u2013264. https:\/\/doi.org\/10.1097\/SCS.0000000000006999","DOI":"10.1097\/SCS.0000000000006999"},{"issue":"1","key":"5788_CR13","doi-asserted-by":"publisher","first-page":"214","DOI":"10.1097\/SCS.0000000000001255","volume":"26","author":"KM Paine","year":"2015","unstructured":"Paine KM, Tahiri Y, Paliga JT, Taylor JA (2015) Simultaneous unicoronal and sagittal distraction osteogenesis for the treatment of nonsyndromic multisutural craniosynostosis. J Craniofac Surg 26(1):214\u2013216. https:\/\/doi.org\/10.1097\/SCS.0000000000001255","journal-title":"J Craniofac Surg"},{"key":"5788_CR14","doi-asserted-by":"publisher","DOI":"10.3389\/fbioe.2022.913190","volume":"10","author":"C Cross","year":"2022","unstructured":"Cross C, Khonsari RH, Patermoster G, Arnaud E, Larysz D, K\u00f6lby L et al (2022) A computational framework to predict calvarial growth: optimising management of sagittal craniosynostosis. Front Bioeng Biotechnol 10:913190. https:\/\/doi.org\/10.3389\/fbioe.2022.913190","journal-title":"Front Bioeng Biotechnol"},{"issue":"5","key":"5788_CR15","doi-asserted-by":"publisher","first-page":"289","DOI":"10.7181\/acfs.2019.00472","volume":"20","author":"HS Yoon","year":"2019","unstructured":"Yoon HS, Na YC, Choi KH, Huh WH, Kim JM (2019) Wound healing effect of regenerated oxidized cellulose versus fibrin sealant patch: an in vivo study. Arch Craniofac Surg 20(5):289\u2013296. https:\/\/doi.org\/10.7181\/acfs.2019.00472","journal-title":"Arch Craniofac Surg"},{"issue":"3","key":"5788_CR16","doi-asserted-by":"publisher","first-page":"357","DOI":"10.1016\/j.cps.2007.04.002","volume":"34","author":"RR Reid","year":"2007","unstructured":"Reid RR (2007) Facial skeletal growth and timing of surgical intervention. Clin Plast Surg 34(3):357\u2013367. https:\/\/doi.org\/10.1016\/j.cps.2007.04.002","journal-title":"Clin Plast Surg"},{"issue":"2","key":"5788_CR17","doi-asserted-by":"publisher","first-page":"167","DOI":"10.1016\/j.coms.2020.01.007","volume":"32","author":"AE Manlove","year":"2020","unstructured":"Manlove AE, Romeo G, Venugopalan SR (2020) Craniofacial growth: current theories and influence on management. Oral Maxillofac Surg Clin North Am 32(2):167\u2013175. https:\/\/doi.org\/10.1016\/j.coms.2020.01.007","journal-title":"Oral Maxillofac Surg Clin North Am"},{"issue":"2","key":"5788_CR18","doi-asserted-by":"publisher","first-page":"133","DOI":"10.1007\/s13353-017-0423-4","volume":"59","author":"A Kutkowska-Ka\u017amierczak","year":"2018","unstructured":"Kutkowska-Ka\u017amierczak A, Gos M, Obersztyn E (2018) Craniosynostosis as a clinical and diagnostic problem: molecular pathology and genetic counseling. J Appl Genet 59(2):133\u2013147. https:\/\/doi.org\/10.1007\/s13353-017-0423-4","journal-title":"J Appl Genet"},{"issue":"R1","key":"5788_CR19","doi-asserted-by":"publisher","first-page":"R107","DOI":"10.1093\/hmg\/ddaa133","volume":"9","author":"R Prasasya","year":"2020","unstructured":"Prasasya R, Grotheer KV, Siracusa LD, Bartolomei MS (2020) Temple syndrome and Kagami-Ogata syndrome: clinical presentations, genotypes, models and mechanisms. Hum Mol Genet 9(R1):R107\u2013R116. https:\/\/doi.org\/10.1093\/hmg\/ddaa133","journal-title":"Hum Mol Genet"},{"issue":"8","key":"5788_CR20","doi-asserted-by":"publisher","first-page":"495","DOI":"10.1136\/jmedgenet-2014-102396","volume":"51","author":"Y Ioannides","year":"2014","unstructured":"Ioannides Y, Lokulo-Sodipe K, Mackay DJ, Davies JH, Temple IK (2014) Temple syndrome: improving the recognition of an underdiagnosed chromosome 14 imprinting disorder: an analysis of 51 published cases. J Med Genet 51(8):495\u2013501. https:\/\/doi.org\/10.1136\/jmedgenet-2014-102396","journal-title":"J Med Genet"},{"issue":"6","key":"5788_CR21","doi-asserted-by":"publisher","first-page":"907","DOI":"10.1016\/j.ajhg.2017.05.006","volume":"100","author":"M Gabriele","year":"2017","unstructured":"Gabriele M, Vulto-van Silfhout AT, Germain PL, Vitriolo A, Kumar R, Douglas E et al (2017) YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction. Am J Hum Genet 100(6):907\u2013925. https:\/\/doi.org\/10.1016\/j.ajhg.2017.05.006","journal-title":"Am J Hum Genet"},{"issue":"4","key":"5788_CR22","doi-asserted-by":"publisher","first-page":"1493","DOI":"10.1111\/j.1471-4159.2008.05486.x","volume":"106","author":"Y He","year":"2008","unstructured":"He Y, Casaccia-Bonnefil P (2008) The Yin and Yang of YY1 in the nervous system. J Neurochem 106(4):1493\u20131502. https:\/\/doi.org\/10.1111\/j.1471-4159.2008.05486.x","journal-title":"J Neurochem"},{"issue":"45","key":"5788_CR23","doi-asserted-by":"publisher","first-page":"46826","DOI":"10.1074\/jbc.M406140200","volume":"279","author":"MJ Morgan","year":"2004","unstructured":"Morgan MJ, Woltering JM, In der Rieden PM, Durston AJ, Thiery JP (2004) YY1 regulates the neural crest-associated slug gene in Xenopus laevis. J Biol Chem 279(45):46826\u201346834. https:\/\/doi.org\/10.1074\/jbc.M406140200","journal-title":"J Biol Chem"},{"issue":"5","key":"5788_CR24","doi-asserted-by":"publisher","first-page":"1213","DOI":"10.1093\/nar\/30.5.1213","volume":"30","author":"DP Tan","year":"2002","unstructured":"Tan DP, Nonaka K, Nuckolls GH, Liu YH, Maxson RE, Slavkin HC, Shum L (2002) YY1 activates Msx2 gene independent of bone morphogenetic protein signaling. Nucleic Acids Res 30(5):1213\u20131223. https:\/\/doi.org\/10.1093\/nar\/30.5.1213","journal-title":"Nucleic Acids Res"},{"key":"5788_CR25","doi-asserted-by":"publisher","unstructured":"Jabs EW, M\u00fcller U, Li X, Ma L, Luo W, Haworth IS et al (1993) A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell 75(3):443\u201350. https:\/\/doi.org\/10.1016\/0092-8674(93)90379-5","DOI":"10.1016\/0092-8674(93)90379-5"},{"key":"5788_CR26","doi-asserted-by":"crossref","unstructured":"Wilkie AO, Tang Z, Elanko N, Walsh S, Twigg SR, Hurst JA et al (2000) Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification. Nat Genet 24(4):387\u201390. https:\/\/doi.org\/10.1038\/74224","DOI":"10.1038\/74224"},{"key":"5788_CR27","doi-asserted-by":"publisher","unstructured":"Punwani D, Zhang Y, Yu J, Cowan MJ, Rana S, Kwan A et al (2016) Multisystem anomalies in severe combined immunodeficiency with mutant BCL11B. N Engl J Med 375(22):2165\u20132176. https:\/\/doi.org\/10.1056\/NEJMoa1509164","DOI":"10.1056\/NEJMoa1509164"},{"issue":"15","key":"5788_CR28","doi-asserted-by":"publisher","first-page":"2501","DOI":"10.1093\/hmg\/ddz072","volume":"28","author":"JAC Goos","year":"2019","unstructured":"Goos JAC, Vogel WK, Mlcochova H, Millard CJ, Esfandiari E, Selman WH et al (2019) A de novo substitution in BCL11B leads to loss of interaction with transcriptional complexes and craniosynostosis. Hum Mol Genet 28(15):2501\u20132513. https:\/\/doi.org\/10.1093\/hmg\/ddz072","journal-title":"Hum Mol Genet"},{"key":"5788_CR29","doi-asserted-by":"publisher","DOI":"10.3389\/fped.2021.772800","volume":"9","author":"L Gaillard","year":"2021","unstructured":"Gaillard L, Goverde A, van den Bosch QCC, Jehee FS, Brosens E, Veenma D et al (2021) Case report and review of the literature: congenital diaphragmatic hernia and craniosynostosis, a coincidence or common cause? Front Pediatr 9:772800. https:\/\/doi.org\/10.3389\/fped.2021.772800","journal-title":"Front Pediatr"},{"key":"5788_CR30","doi-asserted-by":"publisher","DOI":"10.3389\/fped.2022.982361","volume":"10","author":"X Zhao","year":"2022","unstructured":"Zhao X, Wu B, Chen H, Zhang P, Qian Y, Peng X et al (2022) Case report: a novel truncating variant of BCL11B associated with rare feature of craniosynostosis and global developmental delay. Front Pediatr 10:982361. https:\/\/doi.org\/10.3389\/fped.2022.982361","journal-title":"Front Pediatr"},{"key":"5788_CR31","doi-asserted-by":"publisher","unstructured":"Kyrylkova K, Iwaniec UT, Philbrick KA, Leid M (2016) BCL11B regulates sutural patency in the mouse craniofacial skeleton. Dev Biol 415(2):251\u2013260. https:\/\/doi.org\/10.1016\/j.ydbio.2015.10.010","DOI":"10.1016\/j.ydbio.2015.10.010"}],"container-title":["Child's Nervous System"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/s00381-022-05788-x.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/article\/10.1007\/s00381-022-05788-x\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/s00381-022-05788-x.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,8]],"date-time":"2023-05-08T10:07:34Z","timestamp":1683540454000},"score":1,"resource":{"primary":{"URL":"https:\/\/link.springer.com\/10.1007\/s00381-022-05788-x"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,12,13]]},"references-count":31,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2023,5]]}},"alternative-id":["5788"],"URL":"https:\/\/doi.org\/10.1007\/s00381-022-05788-x","relation":{},"ISSN":["0256-7040","1433-0350"],"issn-type":[{"value":"0256-7040","type":"print"},{"value":"1433-0350","type":"electronic"}],"subject":[],"published":{"date-parts":[[2022,12,13]]},"assertion":[{"value":"8 August 2022","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"6 December 2022","order":2,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"13 December 2022","order":3,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}},{"order":1,"name":"Ethics","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"Not applicable.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics approval"}},{"value":"Not applicable.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent to participate"}},{"value":"The patient\u2019s parents provided written informed consent for the publication and the use of the images.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent for publication"}},{"value":"The authors have no relevant financial or non-financial interests to disclose.","order":5,"name":"Ethics","group":{"name":"EthicsHeading","label":"Conflict of interest"}}]}}