cleft lip的例句大全

Hong Kong Association for Cleft Lip and Palate.

香港兔唇裂颚协会工作报告.

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Result the MDSN in the cleft side a unilateral cleft lip nose is lacking.

结果证实单侧完全性唇裂患侧降鼻中隔肌缺损.

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Cleft lip and cleft palate is a kind of common congenital malformation.

唇腭裂是临床上最常见的先天畸形之一.

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Some may also lead to fetal cleft lip, cleft palate, and so on.

有的还可能导致胎儿唇裂 、 腭裂等.

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Results Cleft lip ( CL ): 931 cases ( 19.57 % ), Cleft lip with palate ( CL + P ): 2743 cases ( 57.65 % ), Cleft palate only ( CPO ) : 1084 cases ( 22.78 % ).

结果单纯唇裂 ( cleftlipCL ) 931例 ( 19.57% ), 唇裂伴腭裂(cleftlip with palate CL+P ) 2743 例 ( 57.65% ), 单纯腭裂 ( cleftpalateonlyCPO ) 1084例 ( 22.78% ).

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Methods It based on the understand of pathology anatomise of secondary labionasal deformities after cleft lip repair.

方法：基于对唇裂术后唇鼻畸形病理解剖的认识。

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One-time Operation in Infant Cleft Lip and Palate Plus Alveolar Process

婴儿期一次性手术整复完全性唇腭裂及牙槽突裂

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Methods 40 patients, 19 males and 21 females, with cleft lip and alveolar process only were included. The age range of the patients was from 8 to 33 years with the mean age of 13.8 years when the alveolar bone grafting was performed.

方法40例单侧唇裂合并单纯牙槽突裂患者（19男，21女），手术进行时患者的平均年龄为13.8岁，年龄范围8至33岁。

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Conclusion the authors suggest that the surrounding connective tissues of the atar cartilage play an important role and be the intrinsic basis to produce the characteristic deformities of the cleft lip nose.

结论单侧唇裂形成时这些周边连接组织的组织学差异可能对鼻翼软骨各段扭曲与移位施加了不同的影响，是形成单侧唇裂鼻畸形特征性形态的内在病理解剖学基础。

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To explore the effects of unilateral cleft lip ( UCL) cheiloplasty on nasal deformity.

目的探讨单侧唇裂修复手术对鼻部畸形的治疗影响。

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Objective To find a satisfied repairing method which can complete the functional cheiloplasty while avoiding the visible scar after the cheiloschisis II operation for bilateral cleft lip.

目的探寻一种功能和外观满意，术后上唇不再遗留或减少手术瘢痕的唇裂术后畸形整复方法。

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Objective To explore methods for repairing secondary lip and nasal deformities of unilateral lip cleft.

目的探讨唇裂术后继发鼻部及口唇畸形的整复方法.

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The perinatal birth defects stood on the first 5 rank of incidence list followed by cheiloschisis, cleft lip and cleft palate, hypospadia, congenital hydrocephalus and congenital heart disease.

出生缺陷分类构成的顺位前5位依次为唇裂、唇裂合并腭裂、尿道下裂、先天性脑积水及先天性心脏病；

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Some data also suggest that lack of adequate vitamin B6 or B12 could be a risk factor for cleft lip and cleft palate formation.

有数据表明缺乏足够的维生素B6和B12可能是导致患唇裂和阻碍味觉形成的危险因素。

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Objective: To improve safety and viability of one time operation in the therapy of cleft lip and palate and cleft alveolar process.

目的：探讨婴儿期一次性手术修复完全性唇腭裂及牙槽突裂的安全性与可能性。

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Conclusion: Under the control of provisioned pediatric anesthesia and rehabilitation, one time complete cleft lip and palate plus cleft alveolar process closure is safe and viable.

结论：在专业小儿麻醉及复苏技术保障下，婴儿期一次性手术整复完全性唇腭裂及牙槽突裂是安全可行的。

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Objective To discuss the possibility of surgical repair of congenital cleft lip and alveolar process cleft in neonate stage.

目的探讨新生儿期手术修复先天性唇裂及牙槽突裂的可行性。

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Methods: Under the air vein anesthesia, one time operations were performed in 42 patients with complete cleft lip and palate plus cleft alveolar process.

方法：在气体-静脉复合麻醉下，对42例婴儿完全性唇腭裂及牙槽突裂施行一次性手术整复。

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Surgical Repair of Congenital Cleft Lip and Alveolar Process Cleft in Neonate

新生儿期先天性唇裂及牙槽突裂的外科修复

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Van der Woude syndrome ( VWS, OMIM 119300) is an autosomal dominant craniofacial disorder characterized by pits of the lower lip, hypodontia and cleft lip and/ or cleft palate.

范德伍兹综合征（Van der Woude syndrome，VWS，OMIM119300）是一种常染色体显性遗传病。其特征是家族性下唇瘘复合唇裂或腭裂，1／4的患者伴有缺牙（Hypodontia）。

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