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.
本研究应用电镜免疫细胞化学方法，对小儿先天性巨结肠病结肠壁内含P物质（SP）神经进行了观察。
The ultrastructure of substance P (SP) neuron in the colon of patients with Hirschsprung's disease was investigated by using immunoelectron microscopic method.
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.
应用推荐