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A rare case of bilateral oblique facial cleft and accessory maxilla with repaired unilateral cleft lip and palate

机译:少见的双侧斜面部裂隙和上颌骨伴单侧唇left裂修复

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Cleft lip and palate (CLP) are commonly occurring birth defects which occur due to failure of fusion of various developmental processes of the face, leading to a visible defect in the lip and palate. In severe cases, this defect may extend over the face, thus causing facial clefts. The present case of a 7-year-old girl is unique in the sense that she has right and left side facial clefts of different severity with bilateral accessory maxilla, extra set of dentition, unilateral CLP of the right side, and a double soft palate. Other less associated findings in the case are severe maxillary protrusion, complex open bite, downward and backward rotation of mandible, and incompetent lips with apparently no limb deformities. With some relevant data in hand, we present this case for various suggestions and best possible treatment plan.
机译:唇pa裂(CLP)是常见的先天缺陷,由于面部各种发育过程融合失败而出现,导致唇and裂可见缺陷。在严重的情况下,此缺陷可能会扩展到整个面部,从而导致面部裂痕。本例中的一个7岁女孩在以下方面是独特的,即她的左右面部facial裂程度不同,伴有双侧副上颌骨,额外的牙列,右侧的单侧CLP和双软pa 。该病例其他相关性较弱的结果是上颌严重突突,复杂的开放式咬合,下颌骨向下和向后旋转以及嘴唇无力且明显无肢体畸形。掌握了一些相关数据,我们为这个案例提供了各种建议和最佳的治疗方案。

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