顎関節強直症を伴った骨形成不全症の1例
書誌事項
- タイトル別名
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- Osteogenesis Imperfecta with Temporomandibular Joint Ankylosis: Report of a Case.
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Osteogenesis imperfecta (O. I.) is a generalized hereditary disease characterized by multiple fracture due to bone fragility, blue sclera, auditory disorder, and dentinogenesis imperfecta. In addition, this disease may show hypermobility of joints, scoliosis, and hemorrhagic diathesis.<BR>W e experienced a rare case of O. I. with temporomandibular joint ankylosis recently. The patient was a 27-year-old male with the chief complaint of severe immobility of the mandible caused by a fracture of the right mandibular condyle in his infancy.<BR>In this case, low position arthroplasty was carried out with an excellent result.
収録刊行物
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- 日本口腔科学会雑誌
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日本口腔科学会雑誌 41 (4), 749-754, 1992
特定非営利活動法人 日本口腔科学会
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詳細情報 詳細情報について
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- CRID
- 1390282681412427520
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- NII論文ID
- 130004114246
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- ISSN
- 21850461
- 00290297
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- 本文言語コード
- ja
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- データソース種別
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- JaLC
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可