目的提高对小儿巨结肠类缘病的认识。
Objective To improve the recognition of the intestinal neuronal dysplasia (IND) in children.
总结50例先天性巨结肠患儿的护理。
To summarize the nursing of 50 children with hirschsprung disease.
目的探讨先天性巨结肠症手术治疗的有效术式。
Objective To discuss an effective operation for Hirschsprung, s disease.
目的探讨小儿先天性巨结肠的护理，提高护理质量。
Objective To investigate the nursing of hirschsprung's diseas and thus to raise nursing quality.
总结10例经肛内行先天性巨结肠根治术的护理体会。
In this paper, the authors have concluded the understandings of the nursing of 10 patients with transanal congenital megacolon radical operation.
目的探讨原癌基因RET与先天性巨结肠发生的关系。
Objective To investigate the relationship between RET proto oncogene and the pathogenesis of Hirschsprung′s disease.
目的观察先天性巨结肠肌间神经丛形态学并分析其意义。
Objective To study the morphology of myenteric nerve plexus in the congenital megacolon.
目的：探讨腹腔镜下行先天性巨结肠根治术的临床价值。
Objective: To study the clinical value of Laparoscopy in radical operation on congenital megacolon.
结果：婴儿先天性巨结肠好发于直肠及乙状结肠的交界处。
Results:The infant congenital megacolon often located between rectum and sigmoid.
结论RET基因突变与家族性先天性巨结肠症的发生有关。
Conclusion Mutation of RET proto oncogene might play an role in the familial Hirschsprung's disease.
结论精心的护理在先天性巨结肠的治疗中有着重要的作用。
Conclusion Aborative nurse is very important in Hirschsprung disease treatment.
结肠疾病包括便秘、腹泻、胀气、结肠炎乃至巨结肠和癌等。
Problems involving the colon include ulcerative colitis, constipation and diarrhea, gas discomfort, megacolon (enlarged colon), and cancer.
结果58例先天巨结肠均表现直肠末段不同范围痉挛性狭窄。
Results The X-ray findings of 58 cases of Congenital Megacolon were convulsively strictured segment of rectum end.
目的探讨RET基因的表达情况与先天性巨结肠发生的关系。
Objective to investigate the relationship between the expression of RET proto oncogene and the pathogenesis of Hirschsprung's disease.
结果58例先天性巨结肠均表现为直肠末段不同范围痉挛性狭窄。
Results The radiological findings of 58 children with congenital megacolon were characterized by different range of spastic stricture in rectal end segment.
目的：对29例先天性巨结肠患者手术前后的临床护理及治疗配合。
Objective: To around 29 examples congenital giant colon patient surgery clinical nursing and treatment coordination.
方法分析37例先天性巨结肠术后便秘复发再手术患儿的临床资料。
Methods Clinical data of 37 cases receiving operation again for postoperative constipation recurrences of Hirschsprung disease were collected.
目的比较腹腔镜和剖腹行巨结肠根治术后二组婴儿在临床各方面的特点。
Objective To compare the clinical outcomes of laparoscopy assisted pull through and open operation for Hirschsprung, s Disease (HD) in infants.
报告55例先天性巨结肠病儿，根据不同类型选用不同治疗方法所取得的效果。
This paper reports 55 cases of congenital megacolon, which wore treated by surgical operation or other therapy according to different type of the megacolon.
目的：对新生儿先天性巨结肠根治术两种不同麻醉方法的术后恢复情况进行比较。
Objective:To compare the influence on the postoperative recovery of different anesthesia in congenital Hirschsprung's radical excision in newborn.
方法回顾性分析近2年来行腹腔镜辅助先天性巨结肠根治术12例患者的临床资料。
Methods the clinical data of 12 patients with Hirschsprung disease admitted to our hospital in the last 2 years were retrospectively reviewed.
目的探讨长段型巨结肠及继发扩张肥厚段较长的普通型巨结肠的手术治疗方法及疗效。
Objective To discuss operative methods and treatment for long-segmental HD and secondary lengthen-enlarging-segmental common HD.
采用NADPH二磷酸酶组织化学方法，研究先天性巨结肠症NANC抑制性神经系统。
The nitric oxide synthase(NOS)distribution in the enteric nervous system(NANC inhibition system)was studied by NADPH-diphorase histochemistry method.
目的：探讨相同临床麻醉深度的不同麻醉方法对行腹腔镜先天性巨结肠根治术的婴幼儿的影响。
Objective: To investigate the effect of infant who performed radical operation on congenital megacolon disease in laparoscope under different methods of anaesthesia.
方法应用PCRSSCP银染技术对30例先天性巨结肠原癌基因RET第17外显子进行检测。
Method Exon 17 of RET proto oncogene from 30 children with Hirschsprung's disease was detected by PCR SSCP method.
结论唐氏综合征动物模型16三体鼠伴有先天性巨结肠，这种动物模型可用于研究先天性巨结肠病。
Conclusion trisomy 16 mice occur with congenital megacolon, and trisomy 16 mice may be also regard as an animal model for Hirschsprung's disease.
结论唐氏综合征动物模型16三体鼠伴有先天性巨结肠，这种动物模型可用于研究先天性巨结肠病。
Conclusion trisomy 16 mice occur with congenital megacolon, and trisomy 16 mice may be also regard as an animal model for Hirschsprung's disease.
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