Neurally-mediated Syncope

Overview of Neurally-mediated Syncope

Most recent studies have shown that Neurally-mediated Syncope shares some biological mechanisms with bradycardia, cardiac-arrest, cardiac-arrhythmia, carotid-sinus-syndrome, cerebrovascular-accident, dizziness, epilepsy, heart-diseases, hypotension-adverse-event, neonatal-maladjustment-syndrome, nervousness, pathologic-vasoconstriction, postural-orthostatic-tachycardia-syndrome, presyncope, recurrence-(disease-attribute), syncopal-episodes, syncope, syncope-cardiac, vasovagal-syncope.

Among the many pathways, these few ones have gauged particular interests from scientists studying Neurally-mediated Syncope, and have been seen in publications frequently: Aging, Defecation, Hypersensitivity, Micturition, Pathogenesis, Reflex, Regulation Of Heart Rate, Response To Nitrate, Serotonin Uptake, Short-term Memory, Swimming, Vasoconstriction, Vasodilation

Quite a number of genes have been found to play important roles in Neurally-mediated Syncope, such as ACE, CFH, EPO, FLNA, GNL3, GZMA, KRAS, KRT5, LTF, MEFV, NDUFB6, NMS, POMC, PRL, REN, RGS2, SLC25A5, SLC6A2, SNAI1. 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.

Neurally-mediated Syncope Related Genes

click to see detail information for each gene

Pathways Related to Neurally-mediated Syncope

This information is being compiled and will come in a future update

Related Diseases