{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,20]],"date-time":"2025-11-20T14:42:07Z","timestamp":1763649727445,"version":"3.45.0"},"reference-count":21,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2024,1,27]],"date-time":"2024-01-27T00:00:00Z","timestamp":1706313600000},"content-version":"vor","delay-in-days":26,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Case Reports in Dentistry"],"published-print":{"date-parts":[[2024,1]]},"abstract":"<jats:p>Ectodermal dysplasia is a genetic disorder characterized by the abnormal development of two or more ectodermally driven structures, leading to various clinical manifestations such as sparse hair, dry skin, and hypodontia or anodontia. The absence of teeth significantly impacts the quality of life for individuals affected by this condition. This article presents a clinical case report of a patient with ectodermal dysplasia who underwent full mouth rehabilitation using computer\u2010aided design\/computer\u2010aided manufacturing (CAD\/CAM) technology to fabricate a mandibular complete denture and a maxillary overdenture.<\/jats:p>","DOI":"10.1155\/2024\/9705699","type":"journal-article","created":{"date-parts":[[2024,1,27]],"date-time":"2024-01-27T14:35:07Z","timestamp":1706366107000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Rehabilitation of Ectodermal Dysplasia Using CAD\/CAM Mandibular Complete Denture and Maxillary Overdenture: A Clinical Report"],"prefix":"10.1155","volume":"2024","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9394-3312","authenticated-orcid":false,"given":"Hatem","family":"Alqarni","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Faisal","family":"Alzeghaibi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sahar","family":"Alotaibi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Raghad","family":"Alamri","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Raghad","family":"Aljohani","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Majed S.","family":"Altoman","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mohammed A.","family":"Alfaifi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2024,1,27]]},"reference":[{"key":"e_1_2_6_1_2","doi-asserted-by":"publisher","DOI":"10.1001\/archderm.1990.01670320099019"},{"key":"e_1_2_6_2_2","doi-asserted-by":"publisher","DOI":"10.1111\/jopr.12366"},{"key":"e_1_2_6_3_2","first-page":"285","article-title":"Hypohidrotic ectodermal dysplasia: characteristics and treatment","volume":"26","author":"Kupietzky A.","year":"1995","journal-title":"Quintessence International"},{"key":"e_1_2_6_4_2","doi-asserted-by":"publisher","DOI":"10.5005\/jp-journals-10005-1165"},{"key":"e_1_2_6_5_2","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.28.3.181"},{"key":"e_1_2_6_6_2","first-page":"908","article-title":"A genetic study of anodontia in X- linked hypohidrotic ectodermal dysplasia","volume":"32","author":"Nakata M.","year":"1980","journal-title":"American Journal of Human Genetics"},{"key":"e_1_2_6_7_2","first-page":"25","article-title":"Ectodermal dysplasia: treatment considerations and case reports","volume":"71","author":"Till M. 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