{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,19]],"date-time":"2026-09-19T11:08:32Z","timestamp":1789816112147,"version":"4.0.1"},"reference-count":35,"publisher":"Elsevier BV","issue":"6","license":[{"start":{"date-parts":[[2014,9,1]],"date-time":"2014-09-01T00:00:00Z","timestamp":1409529600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2014,9,1]],"date-time":"2014-09-01T00:00:00Z","timestamp":1409529600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Cranio-Maxillofacial Surgery"],"published-print":{"date-parts":[[2014,9]]},"DOI":"10.1016\/j.jcms.2014.01.037","type":"journal-article","created":{"date-parts":[[2014,1,15]],"date-time":"2014-01-15T04:30:36Z","timestamp":1389760236000},"page":"e346-e351","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":21,"title":["Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation:\u00a0Report of a case and literature review"],"prefix":"10.1016","volume":"42","author":[{"given":"Francois","family":"Clauss","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Etienne","family":"Waltmann","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Philippe","family":"Barriere","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sma\u00efl","family":"Hadj-Rabia","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marie-Cecile","family":"Mani\u00e8re","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Matthieu","family":"Schmittbuhl","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jcms.2014.01.037_bib1","doi-asserted-by":"crossref","first-page":"821","DOI":"10.1086\/520064","article-title":"Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia","volume":"81","author":"Adaimy","year":"2007","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.jcms.2014.01.037_bib2","doi-asserted-by":"crossref","first-page":"96","DOI":"10.4047\/jap.2011.3.2.96","article-title":"Full mouth implant rehabilitation of a patient with ectodermal dysplasia after orthognathic surgery, sinus and ridge augmentation: a clinical report","volume":"3","author":"Bayat","year":"2011","journal-title":"J\u00a0Adv Prosthodont"},{"key":"10.1016\/j.jcms.2014.01.037_bib3","first-page":"520","article-title":"Implant failure in young children with ectodermal dysplasia: a retrospective evaluation of use and outcome of dental implant treatment in children in Sweden","volume":"23","author":"Bergendal","year":"2008","journal-title":"Int J Oral Maxillofac Implants"},{"key":"10.1016\/j.jcms.2014.01.037_bib4","doi-asserted-by":"crossref","first-page":"33","DOI":"10.1007\/s11154-006-9002-4","article-title":"Wnt signaling and osteoblastogenesis","volume":"7","author":"Bodine","year":"2006","journal-title":"Rev Endocr Metab Disord"},{"key":"10.1016\/j.jcms.2014.01.037_bib5","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1016\/j.ajhg.2009.06.001","article-title":"WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes","volume":"85","author":"Bohring","year":"2009","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.jcms.2014.01.037_bib6","doi-asserted-by":"crossref","first-page":"607","DOI":"10.2340\/00015555-0547","article-title":"Sch\u00f6pf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations","volume":"88","author":"Castori","year":"2008","journal-title":"Acta Derm Venereol"},{"key":"10.1016\/j.jcms.2014.01.037_bib7","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1111\/j.1399-0004.2010.01513.x","article-title":"Two families confirm Sch\u00f6pf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum","volume":"79","author":"Castori","year":"2011","journal-title":"Clin Genet"},{"key":"10.1016\/j.jcms.2014.01.037_bib8","doi-asserted-by":"crossref","first-page":"1044","DOI":"10.1111\/j.1365-2133.2010.09670.x","article-title":"Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia cases","volume":"162","author":"Chassaing","year":"2010","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.jcms.2014.01.037_bib9","doi-asserted-by":"crossref","first-page":"1807","DOI":"10.1242\/dev.056051","article-title":"Interactions between Shh, Sostdc1 and Wnt signaling and a new feedback loop for spatial patterning of the teeth","volume":"138","author":"Cho","year":"2011","journal-title":"Development"},{"key":"10.1016\/j.jcms.2014.01.037_bib10","doi-asserted-by":"crossref","first-page":"257","DOI":"10.1111\/j.1399-0004.2010.01376.x","article-title":"X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings","volume":"78","author":"Clauss","year":"2010","journal-title":"Clin Genet"},{"key":"10.1016\/j.jcms.2014.01.037_bib11","doi-asserted-by":"crossref","first-page":"233","DOI":"10.1016\/S0955-0674(99)80031-3","article-title":"Regulation of LEF-1\/TCF transcription factors by Wnt and other signals","volume":"11","author":"Eastman","year":"1999","journal-title":"Curr Opin Cell Biol"},{"key":"10.1016\/j.jcms.2014.01.037_bib12","article-title":"Osseointegration and bone reconstruction in patients affected by ectodermal dysplasia","volume":"108","author":"Garagiola","year":"2006","journal-title":"J\u00a0Cranio-Maxillofacial Surg"},{"key":"10.1016\/j.jcms.2014.01.037_bib13","doi-asserted-by":"crossref","first-page":"1776","DOI":"10.1097\/SCS.0b013e3181f40378","article-title":"Implant treatment in grafted and native bone in patients affected by ectodermal dysplasia","volume":"21","author":"Grecchi","year":"2010","journal-title":"J\u00a0Craniofac Surg"},{"key":"10.1016\/j.jcms.2014.01.037_bib14","doi-asserted-by":"crossref","first-page":"180","DOI":"10.1016\/j.jcms.2013.01.003","article-title":"Leukocyte-platelet-rich plasma (L-PRP) impairs the osteoconductive capacity of the autograft associated to changes in the immunolocalization of TGF-\u03b21 and its co-expression with Wnt10b and CD34","volume":"41","author":"Giovanini","year":"2013","journal-title":"J\u00a0Cranio-Maxillofacial Surg"},{"key":"10.1016\/j.jcms.2014.01.037_bib35","doi-asserted-by":"crossref","first-page":"1119","DOI":"10.1002\/ajmg.a.33840","article-title":"WNT10A and isolated hypodontia","volume":"155","author":"Kantaputra","year":"2011","journal-title":"Am J Med Genet A"},{"key":"10.1016\/j.jcms.2014.01.037_bib15","series-title":"Tissue integrated prostheses","first-page":"199","article-title":"Patient selection and preparation","author":"Lekholm","year":"1985"},{"key":"10.1016\/j.jcms.2014.01.037_bib16","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1126\/scitranslmed.3000231","article-title":"Wnt proteins promote bone regeneration","volume":"2","author":"Minear","year":"2010","journal-title":"Sci Transl Med"},{"key":"10.1016\/j.jcms.2014.01.037_bib17","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.gene.2011.10.044","article-title":"Update on Wnt signaling in bone cell biology and bone disease","volume":"15","author":"Monroe","year":"2012","journal-title":"Gene"},{"key":"10.1016\/j.jcms.2014.01.037_bib18","doi-asserted-by":"crossref","first-page":"220","DOI":"10.1016\/j.jdermsci.2010.03.012","article-title":"Sch\u00f6pf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A","volume":"58","author":"Nagy","year":"2010","journal-title":"J\u00a0Dermatol"},{"key":"10.1016\/j.jcms.2014.01.037_bib19","doi-asserted-by":"crossref","first-page":"1600","DOI":"10.1038\/ejhg.2009.81","article-title":"WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome","volume":"17","author":"Nawaz","year":"2009","journal-title":"Eur J Hum Genet"},{"key":"10.1016\/j.jcms.2014.01.037_bib20","doi-asserted-by":"crossref","first-page":"1010","DOI":"10.1016\/j.bone.2011.07.034","article-title":"High-bone-mass-producing mutations in the Wnt signaling pathway result in distinct skeletal phenotypes","volume":"49","author":"Niziolek","year":"2011","journal-title":"Bone"},{"key":"10.1016\/j.jcms.2014.01.037_bib21","doi-asserted-by":"crossref","first-page":"224","DOI":"10.1111\/j.1440-0960.2011.00788.x","article-title":"Sch\u00f6pf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A","volume":"52","author":"Petrof","year":"2011","journal-title":"Australas J Dermatol"},{"key":"10.1016\/j.jcms.2014.01.037_bib22","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1016\/S0925-4773(01)00452-X","article-title":"Characterization of Wnt gene expression in developing and postnatal hair follicles and identification of Wnt5a as a target of Sonic hedgehog in hair follicle morphogenesis","volume":"107","author":"Reddy","year":"2001","journal-title":"Mech Dev"},{"key":"10.1016\/j.jcms.2014.01.037_bib23","doi-asserted-by":"crossref","first-page":"187","DOI":"10.1016\/j.jcms.2010.04.007","article-title":"Simultaneous maxillary sinus lifting and implant placement with autogenous parietal bone graft: outcome of 17 cases","volume":"39","author":"Sakka","year":"2011","journal-title":"J\u00a0Cranio-Maxillofacial Surg"},{"key":"10.1016\/j.jcms.2014.01.037_bib24","doi-asserted-by":"crossref","first-page":"141","DOI":"10.1111\/j.1365-2443.2008.01258.x","article-title":"Bone morphogenetic protein-2 enhances Wnt\/beta-catenin signaling-induced osteoprotegerin expression","volume":"14","author":"Sato","year":"2009","journal-title":"Genes Cells"},{"key":"10.1016\/j.jcms.2014.01.037_bib25","doi-asserted-by":"crossref","first-page":"235","DOI":"10.1016\/j.jcms.2012.09.007","article-title":"Volume changes of autogenous bone after sinus lifting and grafting procedures: a 6-year computerized tomographic follow-up","volume":"41","author":"Sbordone","year":"2013","journal-title":"J\u00a0Cranio-Maxillofacial Surg"},{"key":"10.1016\/j.jcms.2014.01.037_bib26","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/978-3-540-77727-4_1","article-title":"The role of Wnt signalling in the development of somites and neural crest","volume":"195","author":"Schmidt","year":"2008","journal-title":"Adv Anat Embryol Cell Biol"},{"key":"10.1016\/j.jcms.2014.01.037_bib27","doi-asserted-by":"crossref","first-page":"2014","DOI":"10.1002\/ajmg.a.32991","article-title":"Classifying functional manifestations of ectodermal dysplasias","volume":"149","author":"Simeonsson","year":"2009","journal-title":"Am J Med Genet A"},{"key":"10.1016\/j.jcms.2014.01.037_bib28","doi-asserted-by":"crossref","first-page":"1405","DOI":"10.2741\/e201","article-title":"Role of the Wnt signaling pathway in bone and tooth","volume":"2","author":"Tamura","year":"2010","journal-title":"Front Biosci"},{"key":"10.1016\/j.jcms.2014.01.037_bib29","doi-asserted-by":"crossref","first-page":"1980","DOI":"10.1002\/ajmg.a.32864","article-title":"Ectodermal dysplasias: clinical and molecular review","volume":"149","author":"Visinoni","year":"2009","journal-title":"Am J Med Genet A"},{"key":"10.1016\/j.jcms.2014.01.037_bib30","doi-asserted-by":"crossref","first-page":"673","DOI":"10.1038\/sj.ejhg.5202012","article-title":"Mutation screening of the ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasia","volume":"16","author":"Van der Hout","year":"2008","journal-title":"Eur J Hum Genet"},{"key":"10.1016\/j.jcms.2014.01.037_bib31","doi-asserted-by":"crossref","first-page":"1403","DOI":"10.1111\/j.1365-2133.2010.09703.x","article-title":"Phenotypic variability associated with WNT10A nonsense mutations","volume":"162","author":"Van Geel","year":"2010","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.jcms.2014.01.037_bib32","doi-asserted-by":"crossref","first-page":"1314","DOI":"10.1111\/j.1600-0501.2011.02347.x","article-title":"Bone quality and quantity of the anterior maxillary trabecular bone in dental implant sites","volume":"23","author":"Wakimoto","year":"2012","journal-title":"Clin Oral Implants Res"},{"key":"10.1016\/j.jcms.2014.01.037_bib33","doi-asserted-by":"crossref","first-page":"346","DOI":"10.2340\/00015555-1028","article-title":"Intra-familial variability of ectodermal defects associated with WNT10A mutations","volume":"91","author":"Wedgeworth","year":"2011","journal-title":"Acta Derm Venereol"},{"key":"10.1016\/j.jcms.2014.01.037_bib34","doi-asserted-by":"crossref","first-page":"49","DOI":"10.1016\/j.devcel.2009.05.011","article-title":"Reciprocal requirements for EDA\/EDAR\/NF-kappaB and Wnt\/beta-catenin signaling pathways in hair follicle induction","volume":"17","author":"Zhang","year":"2009","journal-title":"Dev Cell"}],"container-title":["Journal of Cranio-Maxillofacial Surgery"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1010518214000390?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1010518214000390?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T14:32:09Z","timestamp":1760884329000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1010518214000390"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,9]]},"references-count":35,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2014,9]]}},"alternative-id":["S1010518214000390"],"URL":"https:\/\/doi.org\/10.1016\/j.jcms.2014.01.037","relation":{},"ISSN":["1010-5182"],"issn-type":[{"value":"1010-5182","type":"print"}],"subject":[],"published":{"date-parts":[[2014,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation:\u00a0Report of a case and literature review","name":"articletitle","label":"Article Title"},{"value":"Journal of Cranio-Maxillofacial Surgery","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jcms.2014.01.037","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2014 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}