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Disease Info Card
Velopharyngeal Insufficiency
Information about Velopharyngeal Insufficiency: 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 Velopharyngeal Insufficiency
Most recent studies have shown that Velopharyngeal Insufficiency shares some biological mechanisms with airway-obstruction, apnea, articulation-disorders, cleft-lip, cleft-palate, cleft-palate-with-cleft-lip, congenital-abnormality, congenital-heart-defects, digeorge-syndrome, hemorrhage, hypernasality, nasopharyngeal-diseases, pathologic-fistula, sleep-apnea-obstructive, sleep-apnea-syndromes, snoring, speech-disorders, submucous-cleft-of-hard-palate, voice-disorders.
Among the many pathways, these few ones have gauged particular interests from scientists studying Velopharyngeal Insufficiency, and have been seen in publications frequently: Aging, Brain Development, Coagulation, Cognition, Dehiscence, Hemostasis, Innervation, Interphase, Localization, Mastication, Metaphase, Muscle Adaptation, Muscle Contraction, Ossification, Palate Development, Pathogenesis, Reflex, Transport, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Velopharyngeal Insufficiency, such as AVP, CALML3, CENPJ, CNTN1, COTL1, CP, CSRP3, F3, FUT3, HPS4, PDXP, PLP1, PPOX, PRDX5, PTHLH, SMCP, TBX1, TFF2. 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.