1) Anorectoplasty
肛门直肠成形术
2) anorectoplasty
肛门成形术
1.
Objective: To evaluate the therapeutic effect of posterior transversal anorectoplasty on high or medial anorectal abnormalities.
目的:了解经尾部横切口肛门成形术治疗高、中位肛门直肠畸形疗效。
3) Surgery of Anorectal Diseases
肛门直肠手术
1.
Curative Effect Observation about Longbishu Capsule with Harnal Combined in Pretenting the Urinary Retention after Surgery of Anorectal Diseases
癃闭舒胶囊联合哈乐预防肛门直肠手术后尿潴留的临床观察
4) anorectal anomalies
肛门直肠畸形
1.
Anterior sagittal anorectoplasty for treatment of 48 patients with anorectal anomalies;
前矢状入路治疗肛门直肠畸形48例
2.
Objective To explore atechnical modification bytransperineal Da-Wanorectoplasty(Da-WARP) ontreatinglow,intermedi-ate anorectal anomalies(AA) andto evaluate the results of long-termfollowup.
目的探讨经会阴(大-W)手术方法治疗中、低位肛门直肠畸形(AA)的价值,对其长期疗效进行评价。
5) anorectal malformation
肛门直肠畸形
1.
Complications and countermeasures of Pea's procedure to treat meta-superior position anorectal malformation;
Pea术式治疗中高位肛门直肠畸形的并发症及对策
2.
Anorectoplasty via posterior sagittal approach in treatment of anorectal malformation of medium and highly seated: report of 44 cases;
经后矢状入路肛门直肠成形术治疗中高位肛门直肠畸形疗效分析
3.
Anorectal malformation and accompanied malformations in rat fetuses induced by retinoic acid;
维甲酸诱导大鼠产生肛门直肠畸形及其伴发畸形
6) anorectal malformations
肛门直肠畸形
1.
Objective To observe the pathologic changes of ganglion cell and nerve plexus in internal anus sphincter of rats with congenital anorectal malformations (ARM).
目的观察肛门直肠畸形动物模型肛门内括约肌肌间神经节细胞及神经丛的数目和形态。
2.
Anorectal malformations represent a spectrum of anomalities from the very minor in covered anus to the more extreme cloaca and their pathologic variations are very complex.
前言 先天性肛门直肠畸形(Congenital anorectal malformations, ARMs)是常见的消化道畸形,其发生率在,1500—5000名新生儿中一例。
3.
Objective To investigate the expression and effective of Sonic hedgehog(Shh)gene during anorectum development in ethylenethiourea(ETU)-exposed embryos with anorectal malformations.
Shh基因表达在肛门直肠及其畸形发生过程中发挥重要作用,ETU可能影响Shh信号转导系统和肛门直肠畸形发生。
补充资料：肛门直肠脱垂
肛门直肠脱垂
proctoptosis
简称“脱肛”。指肛管、直肠外翻而脱垂于肛门外。小儿较成人多见。尤多见于1～3岁小儿，5岁以后则罕见。病因：①解剖上发育缺陷。②支持直肠的组织软弱。③长时期腹内压增加。仅有黏膜脱出者称为不完全脱肛。肠管各层完全翻出者称为完全脱肛。一般采取保守疗法即愈。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条