{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,12]],"date-time":"2025-10-12T01:55:53Z","timestamp":1760234153285,"version":"build-2065373602"},"reference-count":32,"publisher":"MDPI AG","issue":"8","license":[{"start":{"date-parts":[[2021,4,15]],"date-time":"2021-04-15T00:00:00Z","timestamp":1618444800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["IJERPH"],"abstract":"<jats:p>Osteogenesis imperfecta describes a group of genetic disorders that result from a defect in collagen type I and range in severity from a subtle increase in fracture frequency to death in the perinatal period. Osteogenesis imperfecta is mostly caused by mutations in the COL1A1 (17q21.33) and COL1A2 (7q21.3) genes. There have only been a few case reports of implant-prosthetic treatment for patients with osteogenesis imperfecta. These reports indicated that implants and augmentation procedures can be implemented in such patients. However, for patients receiving additional antiresorptive therapy, cautious approaches should be chosen and the risk of drug-associated osteonecrosis should be considered. The aim of this article is to report on the implant-prosthetic treatment of a patient with type I osteogenesis imperfecta.<\/jats:p>","DOI":"10.3390\/ijerph18084169","type":"journal-article","created":{"date-parts":[[2021,4,15]],"date-time":"2021-04-15T12:11:00Z","timestamp":1618488660000},"page":"4169","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["Implant-Prosthetic Restoration of a Patient with Osteogenesis Imperfecta: A Case Report"],"prefix":"10.3390","volume":"18","author":[{"given":"Marcel","family":"Hanisch","sequence":"first","affiliation":[{"name":"Research Unit Rare Diseases with Orofacial Manifestations, Department of Cranio-Maxillofacial Surgery, Albert-Schweitzer-Campus 1, University Hospital M\u00fcnster, Building W 30, D-48149 M\u00fcnster, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Melanie","family":"Maus","sequence":"additional","affiliation":[{"name":"Research Unit Rare Diseases with Orofacial Manifestations, Department of Cranio-Maxillofacial Surgery, Albert-Schweitzer-Campus 1, University Hospital M\u00fcnster, Building W 30, D-48149 M\u00fcnster, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Johannes","family":"Kleinheinz","sequence":"additional","affiliation":[{"name":"Research Unit Rare Diseases with Orofacial Manifestations, Department of Cranio-Maxillofacial Surgery, Albert-Schweitzer-Campus 1, University Hospital M\u00fcnster, Building W 30, D-48149 M\u00fcnster, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1968","published-online":{"date-parts":[[2021,4,15]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1016\/j.metabol.2017.06.001","article-title":"Osteogenesis imperfecta\u2014A clinical update","volume":"80","author":"Tournis","year":"2018","journal-title":"Metabolism"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1038\/ejhg.2011.141","article-title":"EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfecta","volume":"20","author":"Byers","year":"2012","journal-title":"Eur. 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