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Disease Info Card
Currarino Triad
Information about Currarino Triad: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Currarino Triad
Most recent studies have shown that Currarino Triad shares some biological mechanisms with anorectal-anomaly, anorectal-stricture, anus-imperforate, chronic-constipation, congenital-abnormality, congenital-absence, congenital-digestive-system-anomalies, congenital-sacral-meningocele, constipation, hirschsprung-disease, meningitis, meningocele, neoplasms, pathologic-fistula, sacral-agenesis, spinal-neoplasms, stenosis, stricture-of-anus, syringomyelia, teratoma.
Among the many pathways, these few ones have gauged particular interests from scientists studying Currarino Triad, and have been seen in publications frequently: Defecation, Localization, Neural Tube Closure, Pathogenesis, Transposition, Tube Closure
Quite a number of genes have been found to play important roles in Currarino Triad, such as CALR, CS, CSF2, ENDOU, EXOSC6, FXN, HTT, LAMC2, MNX1, MTSS1, OXA1L, PSMD3, RET, RPS3, SHH. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.
Pathways Related to Currarino Triad
This information is being compiled and will come in a future update
| Defecation | Localization | Neural Tube Closure |
| Pathogenesis | Transposition | Tube Closure |