Disease Info Card

Articulation Disorders

Information about Articulation Disorders: 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 Articulation Disorders

Most recent studies have shown that Articulation Disorders shares some biological mechanisms with aphasia, apraxias, cleft-lip, cleft-palate, cleft-palate-with-cleft-lip, complete-hearing-loss, deglutition-disorders, developmental-reading-disorder, dysarthria, dyslexia, hypernasality, impairment-(finding), language-development-disorders, language-disorders, malnutrition, malocclusion, speech-disorders, stuttering, velopharyngeal-insufficiency, voice-disorders.

Among the many pathways, these few ones have gauged particular interests from scientists studying Articulation Disorders, and have been seen in publications frequently: Aging, Bone Resorption, Brain Development, Cognition, Dehiscence, Developmental Process, Lactation, Localization, Long-term Memory, Mastication, Proprioception, Reflex, Righting Reflex, Rumination, Segmentation, Short-term Memory, Tooth Eruption, Translation, Transposition, Wound Healing

Quite a number of genes have been found to play important roles in Articulation Disorders, such as BLOC1S6, CNTN1, CP, ERMAP, EXOSC10, F2, F3, FAS, FASN, FOXP2, HNRNPC, NDUFB6, PEX7, PHYH, PRH1, 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.