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Polymorphisms in the genes encoding the 4 RET ligands, GDNF, NTN, ARTN, PSPN, and susceptibility to Hirschsprung disease
|Authors:||Fernández, Raquel M.; Ruiz-Ferrer, Macarena; López-Alonso, Manuel; Antiñolo, Guillermo ; Borrego, Salud|
|Keywords:||Hirschsprung disease (HSCR)|
|Citation:||Journal of Pediatric Surgery 43(11): 2042-2047 (2008)|
|Abstract:||[Purpose] Hirschsprung disease (HSCR) is a developmental disorder caused by a failure of neural crest cells to migrate, proliferate, and/or differentiate during the enteric nervous system development. It presents a multifactorial, nonmendelian pattern of inheritance, with several genes playing some role in its pathogenesis. Its major susceptibility gene is the RET protooncogene, which encodes a receptor tyrosine kinase activating several key signaling pathways in the enteric nervous system development. Given the pivotal role of RET in HSCR, the genes encoding their ligands (GDNF, NRTN, ARTN, and PSPN) are also good candidates for the disease.|
[Methods] We have performed a case-control study using Taqman technology to evaluate 10 polymorphisms within these genes, as well as haplotypes comprising them, as susceptibility factors for HSCR.
[Result] No differences were found in the allelic frequencies of the variants or in the haplotype distribution between patients and controls. In addition, no particular association was detected of the variants/haplotypes to any demographic/clinical parameters within the group of patients.
[Conclusion] These data would be consistent with the lack of association between these polymorphisms and HSCR, although they do not permit to completely discard a possible role of other variants within these genes in the disease. Moreover, because the gene-by-gene approach does not take into account the polygenic nature of HSCR disease, it would be interesting to investigate sets of variants in many other different susceptibility loci described for HSCR, which may permit to consider possible interactions among susceptibility genes.
|Description:||6 pages, 3 tables.-- PMID: 18970938 [PubMed].-- Printed version published Nov 2008.|
|Publisher version (URL):||http://dx.doi.org/10.1016/j.jpedsurg.2008.05.018|
|Appears in Collections:||(IBIS) Artículos|
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