Osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings
Journal of the Korean Association of Oral and Maxillofacial Surgeons
; : 70-77, 2020.
Article
in En
| WPRIM
| ID: wpr-811266
Responsible library:
WPRO
ABSTRACT
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.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Orthodontics
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Osteogenesis
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Osteogenesis Imperfecta
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Prognathism
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Congenital Abnormalities
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Connective Tissue Diseases
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Siblings
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Facial Asymmetry
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Orthognathic Surgery
Limits:
Humans
Language:
En
Journal:
Journal of the Korean Association of Oral and Maxillofacial Surgeons
Year:
2020
Type:
Article