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Disease Info Card
Pallister-hall Syndrome
Information about Pallister-hall 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 Pallister-hall Syndrome
Most recent studies have shown that Pallister-hall Syndrome shares some biological mechanisms with anus-imperforate, chromosomal-translocation, congenital-abnormality, congenital-heart-defects, greig-cephalopolysyndactyly-syndrome, hamartoma, haploinsufficiency, holoprosencephaly, hypopituitarism, hypothalamic-diseases, hypothalamic-hamartoma, hypothalamic-neoplasms, limb-deformities-congenital, neoplasms, pituitary-diseases, polydactyly, polysyndactyly, syndactyly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Pallister-hall Syndrome, and have been seen in publications frequently: Aging, Brain Development, Cell Development, Cell Differentiation, Cell Migration, Ectoderm Development, Epithelial Cell Differentiation, Kidney Development, Limb Development, Localization, Lymphocyte Differentiation, Muscle Cell Differentiation, Pathogenesis, Peristalsis, Regeneration, Secretion, Segmentation, Smooth Muscle Cell Differentiation, Transport, Ureter Morphogenesis
Quite a number of genes have been found to play important roles in Pallister-hall Syndrome, such as CCM2, FUT1, GAS1, GGH, GH1, GLI1, GLI3, HFE, IKZF1, LRP2, NDUFB6, PCBD1, POMC, PTCH1, SHH, SMO, SMOX. 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.