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
相关论文
共 104 条
  • [1] FAMILIAL JEJUNAL ATRESIA WITH APPLE-PEEL VARIANT
    ALAWADI, SA
    NAGUIB, K
    ISSA, M
    FARAG, TI
    CUSCHIERI, A
    [J]. JOURNAL OF THE ROYAL SOCIETY OF MEDICINE, 1981, 74 (07) : 499 - 501
  • [2] Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease
    Amiel, J
    Attie, T
    Jan, D
    Pelet, A
    Edery, P
    Bidaud, C
    Lacombe, D
    Tam, P
    Simeoni, J
    Flori, E
    NihoulFekete, C
    Munnich, A
    Lyonnet, S
    [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (03) : 355 - 357
  • [3] Genetic polymorphisms of cyclooxygenase-1 (COX-1) are associated with functional dyspepsia in Japanese women
    Arisawa, Tomiyasu
    Tahara, Tomomitsu
    Shibata, Tomoyuki
    Nagasaka, Mitsuo
    Nakamura, Masakatsu
    Kamiya, Yoshio
    Fujita, Hiroshi
    Yoshioka, Daisuke
    Arima, Yuko
    Okub, Masaaki
    Hirata, Ichiro
    Nakano, Hiroshi
    [J]. JOURNAL OF WOMENS HEALTH, 2008, 17 (06) : 1039 - 1043
  • [4] Arisawa T, 2007, INT J MOL MED, V20, P717
  • [5] DIVERSITY OF RET PROTOONCOGENE MUTATIONS IN FAMILIAL AND SPORADIC HIRSCHSPRUNG DISEASE
    ATTIE, T
    PELET, A
    EDERY, P
    ENG, C
    MULLIGAN, LM
    AMIEL, J
    BOUTRAND, L
    BELDJORD, C
    NIHOULFEKETE, C
    MUNNICH, A
    PONDER, BAJ
    LYONNET, S
    [J]. HUMAN MOLECULAR GENETICS, 1995, 4 (08) : 1381 - 1386
  • [6] IDENTIFICATION OF HUMAN ACTIVIN AND TGF-BETA TYPE-I RECEPTORS THAT FORM HETEROMERIC KINASE COMPLEXES WITH TYPE-II RECEPTORS
    ATTISANO, L
    CARCAMO, J
    VENTURA, F
    WEIS, FMB
    MASSAGUE, J
    WRANA, JL
    [J]. CELL, 1993, 75 (04) : 671 - 680
  • [7] Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population
    Auricchio, A
    Casari, G
    Staiano, A
    Ballabio, A
    [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (03) : 351 - 354
  • [8] Bassett WD, 2008, J CLIN GASTROENTEROL, V42, P720, DOI 10.1097/MCG.0b013e3181646730
  • [9] PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD)
    Bergmann, C
    Senderek, J
    Küpper, F
    Schneider, F
    Dornia, C
    Windelen, E
    Eggermann, T
    Rudnik-Schöneborn, S
    Kirfel, J
    Furu, L
    Onuchic, LE
    Rossetti, S
    Harris, PC
    Somlo, S
    Guay-Woodford, L
    Germino, GG
    Moser, M
    Büttner, R
    Zerres, K
    [J]. HUMAN MUTATION, 2004, 23 (05) : 453 - 463
  • [10] Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease
    Bidaud, C
    Salomon, R
    VanCamp, G
    Pelet, A
    Attie, T
    Eng, C
    Bonduelle, M
    Amiel, J
    NihoulFekete, C
    Willems, PJ
    Munnich, A
    Lyonnet, S
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 1997, 5 (04) : 247 - 251