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Disease Info Card
Hypernasality
Information about Hypernasality: 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 Hypernasality
Most recent studies have shown that Hypernasality shares some biological mechanisms with articulation-disorders, cleft-lip, cleft-palate, cleft-palate-with-cleft-lip, deglutition-disorders, digeorge-syndrome, dysarthria, hyponasality, nasal-air-emission, nasopharyngeal-diseases, oral-fistula, pathologic-fistula, regurgitation, rhinolalias, speech-disorders, submucous-cleft-of-hard-palate, unilateral-cleft-lip, velopharyngeal-insufficiency, voice-disorders.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hypernasality, and have been seen in publications frequently: Aging, Dehiscence, Eating Behavior, Mastication, Pathogenesis, Reflex, Secretion, Transport, Transposition
Quite a number of genes have been found to play important roles in Hypernasality, such as AVP, CADPS, CALML3, CAPS, CENPJ, CNTN1, COTL1, CP, CPO, CPOX, CSRP3, FUT3, GLI3, HPS4, PAPPA, PPOX, SMCP, TMEM54, TTF2. 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.
Pathways Related to Hypernasality
This information is being compiled and will come in a future update
| Aging | Dehiscence | Eating Behavior |
| Mastication | Pathogenesis | Reflex |
| Secretion | Transport | Transposition |