書誌事項
- タイトル別名
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- Oro-Facial Findings of a Patient with Rieger's Syndrome
この論文をさがす
抄録
Rieger's Syndrome is an autosomal-dominant heritable disorder with triad of hypoplasia of the anterior iris stroma, bridging angle of the iris strands and posterior embryotoxon. Other various clinical findings were manifested due to abnormal development of the mesodermal tissue. The present findings of a sixyearold boy affected with Rieger's Syndrome were as follows.<BR>1. Three irregular pupilla, cloudy cornea and auricular septal defects.<BR>2. Low body height and delay of bone age.<BR>3. Microdontia of the lateral upper incisors and delay of calcification of the upper second premolars<BR>.4. Hypoplasia of the maxilla and anterior crossbite.<BR>5. Occlusal correction of the anterior crossbite using a Frankel type III unit.
収録刊行物
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- The Japanese Journal of Pediatric Dentistry
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The Japanese Journal of Pediatric Dentistry 32 (4), 889-896, 1994
The Japanese Society of Pediatric Dentistry
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詳細情報 詳細情報について
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- CRID
- 1390282679662000000
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- NII論文ID
- 130004633055
- 50005478892
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- ISSN
- 05831199
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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