论文部分内容阅读
儿童型早老症(又称Hutchinson-Gilf(?)-rd 综合症)于1886年Hutchinson 首次报道,不久Gilf(?)rd 发表1例尸检报告。本症特征危及小儿生长发育,表现进行性退行性衰老改变。本症罕见,为研究人类衰老机制,提供了极好模式。本院于1983年2月在浙江省余杭县发现1例,已随访3年半,现报告如下.病例介绍病史:张×,男,10岁。母孕期正常,
Hutchinson’s first report of childhood neoplasia (also known as Hutchinson-Gilf®-rd syndrome) was first reported in 1886 and Gilf (R) rd published an autopsy report shortly thereafter. The disease characteristics endanger the growth and development of children, the performance of progressive degenerative changes in aging. The disease is rare, for the study of human aging mechanism, provides an excellent model. The hospital in February 1983 in Yuhang County, Zhejiang Province found in 1 case, has been followed for 3 years and a half, are as follows. Case description History: Zhang ×, male, 10 years old. Mother during pregnancy normal,