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Disease Info Card
Caudal Regression Syndrome
Information about Caudal Regression Syndrome: 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 Caudal Regression Syndrome
Most recent studies have shown that Caudal Regression Syndrome shares some biological mechanisms with anorectal-anomaly, anus-imperforate, atresia, congenital-abnormality, congenital-absence, congenital-absence-of-kidney, diabetes-mellitus, diabetes-mellitus-insulin-dependent, dysplasia, lipoma, meningomyelocele, neurogenic-urinary-bladder, pathologic-fistula, pregnancy-in-diabetics, sacral-agenesis, sirenomelia, spina-bifida, syringomyelia, urogenital-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Caudal Regression Syndrome, and have been seen in publications frequently: Blood Coagulation, Cell Death, Cell Division, Cell Proliferation, Cellular Localization, Coagulation, Embryo Development, Innervation, Kidney Development, Localization, Mesoderm Formation, Micturition, Mrna Splicing, Organ Formation, Ossification, Pathogenesis, Segmentation, Tissue Remodeling, Transposition
Quite a number of genes have been found to play important roles in Caudal Regression Syndrome, such as ACD, CALCA, CD2, CD38, CYP26A1, DACT1, GDF11, INS, MNX1, NPY, PCSK5, PGPEP1, PSMC1, PSMD1, PSMD3, RBP1, RPS3, RPS4Y1. 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.