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Disease Info Card
Sturge-weber Syndrome
Information about Sturge-weber 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 Sturge-weber Syndrome
Most recent studies have shown that Sturge-weber Syndrome shares some biological mechanisms with angiomatosis, apnea, brain-diseases, calcinosis, depressive-disorder, epilepsy, glaucoma, hemangioma, klippel-trenaunay-weber-syndrome, melanocytic-nevus, neoplasms, nervousness, neurocutaneous-syndromes, port-wine-stain, sleep-apnea-syndromes, sleep-disorders, sleeplessness, tuberous-sclerosis, vascular-anomaly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Sturge-weber Syndrome, and have been seen in publications frequently: Aging, Angiogenesis, Circadian Rhythm, Cognition, Cortisol Secretion, Excretion, Glomerular Filtration, Growth Hormone Secretion, Habituation, Homeostatic Process, Hormone Secretion, Innervation, Localization, Locomotion, Long-term Memory, Myelination, Pathogenesis, Reflex, Secretion, Transport
Quite a number of genes have been found to play important roles in Sturge-weber Syndrome, such as CAT, CRAT, CRH, CTNNBL1, GGH, GH1, GHRH, GLYAT, ITSN2, LIFR, PNPLA6, POMC, RANGAP1, REM1, SLC17A5, TNF, TNFSF14, TST. 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.