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Osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings
Osteogenesis imperfecta is a heterogeneous group of connective tissue diseases that is predominantly characterized by bone fragility and skeletal deformity. Two siblings with undiagnosed type I osteogenesis imperfecta underwent orthognathic surgery for the treatment of facial asymmetry and mandibula...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Association of Oral and Maxillofacial Surgeons
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049766/ https://www.ncbi.nlm.nih.gov/pubmed/32158684 http://dx.doi.org/10.5125/jkaoms.2020.46.1.70 |
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author | Kim, Dong-Young Baik, Unbong Jeon, Ju-Hong |
author_facet | Kim, Dong-Young Baik, Unbong Jeon, Ju-Hong |
author_sort | Kim, Dong-Young |
collection | PubMed |
description | Osteogenesis imperfecta is a heterogeneous group of connective tissue diseases that is predominantly characterized by bone fragility and skeletal deformity. Two siblings with undiagnosed type I osteogenesis imperfecta underwent orthognathic surgery for the treatment of facial asymmetry and mandibular prognathism. The authors report two cases of combined orthodontics and orthognathic surgery in patients with type I osteogenesis imperfecta, mandibular prognathism, and facial asymmetry. |
format | Online Article Text |
id | pubmed-7049766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Korean Association of Oral and Maxillofacial Surgeons |
record_format | MEDLINE/PubMed |
spelling | pubmed-70497662020-03-10 Osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings Kim, Dong-Young Baik, Unbong Jeon, Ju-Hong J Korean Assoc Oral Maxillofac Surg Case Report Osteogenesis imperfecta is a heterogeneous group of connective tissue diseases that is predominantly characterized by bone fragility and skeletal deformity. Two siblings with undiagnosed type I osteogenesis imperfecta underwent orthognathic surgery for the treatment of facial asymmetry and mandibular prognathism. The authors report two cases of combined orthodontics and orthognathic surgery in patients with type I osteogenesis imperfecta, mandibular prognathism, and facial asymmetry. The Korean Association of Oral and Maxillofacial Surgeons 2020-02 2020-02-26 /pmc/articles/PMC7049766/ /pubmed/32158684 http://dx.doi.org/10.5125/jkaoms.2020.46.1.70 Text en Copyright © 2020 The Korean Association of Oral and Maxillofacial Surgeons. http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kim, Dong-Young Baik, Unbong Jeon, Ju-Hong Osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings |
title | Osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings |
title_full | Osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings |
title_fullStr | Osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings |
title_full_unstemmed | Osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings |
title_short | Osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings |
title_sort | osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049766/ https://www.ncbi.nlm.nih.gov/pubmed/32158684 http://dx.doi.org/10.5125/jkaoms.2020.46.1.70 |
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