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.
机构:
Alder Hey Childrens NHS Fdn Trust, Dept Paediat Surg, Liverpool L12 2AP, Merseyside, England
Univ Liverpool, Div Reprod & Dev Med, Liverpool L69 3BX, Merseyside, EnglandAlder Hey Childrens NHS Fdn Trust, Dept Paediat Surg, Liverpool L12 2AP, Merseyside, England
Kenny, Simon E.
Tam, Paul K. H.
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h-index: 0
机构:
Univ Hong Kong, Li Ka Shing Fac Med, Dept Surg, Hong Kong, Hong Kong, Peoples R ChinaAlder Hey Childrens NHS Fdn Trust, Dept Paediat Surg, Liverpool L12 2AP, Merseyside, England
Tam, Paul K. H.
Garcia-Barcelo, Merce
论文数: 0引用数: 0
h-index: 0
机构:
Univ Hong Kong, Li Ka Shing Fac Med, Dept Surg, Hong Kong, Hong Kong, Peoples R ChinaAlder Hey Childrens NHS Fdn Trust, Dept Paediat Surg, Liverpool L12 2AP, Merseyside, England
机构:
Paracelsus Med Privatuniv PMU, Univ Klin Kinder & Jugendchirurg, Zentrum Kinder & Jugendmed, Salzburger Landeskliniken SALK, Mullner Hauptstr 48, A-5020 Salzburg, AustriaParacelsus Med Privatuniv PMU, Univ Klin Kinder & Jugendchirurg, Zentrum Kinder & Jugendmed, Salzburger Landeskliniken SALK, Mullner Hauptstr 48, A-5020 Salzburg, Austria