Hirschsprung's disease as a neurochristopathy

被引:0
作者
Martucciello, G
机构
关键词
Hirschsprung's disease; neurocristopathies; RET proto-oncogene;
D O I
暂无
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Recent molecular-genetic and histochemical studies of intestinal aganglionosis have confirmed the initial classification established by Bolande, who considered Hirschsprng's disease (HD) a neurocristopathy. This paper is a critical review of the results of molecular-genetic studies carried out from 1992 to date. In particular, the author focuses on the possible clinical impact of the identification of RET as a causative gene for HD.
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页码:2 / 10
页数:9
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