Genetic testing in other GI diseases

被引:2
|
作者
Hodgson, Shirley [2 ]
Ioannides, Adonis S. [1 ]
机构
[1] Great Ormond St Hosp Sick Children, Clin Genet Unit, London WC1N 3JH, England
[2] Univ London, London WC1E 7HU, England
关键词
Gastrointestinal; genetics; malformations; disorders; diseases; testing; RET PROTOONCOGENE; HIRSCHSPRUNG DISEASE; CHRONIC-PANCREATITIS; INTERSTITIAL DELETION; ESOPHAGEAL ATRESIA; ENDOTHELIN-3; GENE; BILIARY ATRESIA; JEJUNAL ATRESIA; N34S MUTATION; LIVER-DISEASE;
D O I
10.1016/j.bpg.2009.02.008
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Gastrointestinal development is a complex process comprising folding of the endodermal layer to form the primitive gut tube, cell differentiation along its anteroposterior axis, the budding of the various organ primordia and development of derivative organs like the liver and pancreas and the colonisation of the gut with neuronal precursors. Genetic factors are increasingly recognised as playing a significant role in the disturbance of this developmental process which underlies congenital malformations and gastrointestinal disorders. Furthermore, genetic variation and its interaction with environmental influences play an important role in the pathogenesis of functional gastrointestinal disorders. In this review, we discuss the contribution of genetic variants, ranging from highly penetrant mutations and chromosomal abnormalities to genetic polymorphisms, to the pathogenesis of a number of structural and functional gastrointestinal disorders. (C) 2009 Published by Elsevier Ltd.
引用
收藏
页码:245 / 256
页数:12
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