多重 の 歯 の 影響 と 歯 の 胞子 を 伴う クレイドクロニアル ディスプラシア: 希少 な 組織 の 症例 報告
1Department of Dentistry, Adesh Institute of Dental Sciences and Research, Bathinda, IND.
Cureus
|September 2, 2025
まとめ
クレイドクロニアル不形成症 (CCD) は希少な遺伝疾患である. この症例は,CCD患者における 広範囲に及ぶ歯とキストを強調し, 多分野治療の必要性を強調しています.
科学分野:
- 遺伝学と発達生物学
- 口腔・口腔外科
- 矯正 矯正 矯正 矯正 矯正 矯正 矯正
背景:
- 骨格および歯の異常が特徴で,主に骨や歯の発達に影響する珍しい自己相性優位性遺伝疾患である.
- この状態は,骨格細胞の分化と骨格形態変異に不可欠なRunt関連転写因子2 (RUNX2) 遺伝子の変異によって引き起こされます.
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