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Disease Info Card
Spasmodic Dysphonia
Information about Spasmodic Dysphonia: 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 Spasmodic Dysphonia
Most recent studies have shown that Spasmodic Dysphonia shares some biological mechanisms with adductor-spastic-dysphonia, blepharospasm, deglutition-disorders, dystonia-disorders, focal-dystonia, laryngeal-diseases, laryngismus, movement-disorders, muscle-spasticity, spasm, speech-disorders, torticollis, vocal-cord-paralysis, voice-disorders.
Among the many pathways, these few ones have gauged particular interests from scientists studying Spasmodic Dysphonia, and have been seen in publications frequently: Aging, Anaphylaxis, Cell Adhesion, Cell Proliferation, Coagulation, Hemostasis, Innervation, Involuntary Skeletal Muscle Contraction, Localization, Muscle Atrophy, Muscle Contraction, Parturition, Pathogenesis, Reflex, Regeneration, Skeletal Muscle Contraction, Translation, Transport
Quite a number of genes have been found to play important roles in Spasmodic Dysphonia, such as ABR, BTN1A1, CAMP, CD1B, CD1E, CD82, FLVCR1, PDE8B, RANGAP1, RRM2, SLC17A5, SLC4A7, SPTBN2, THAP1, TOR1A. 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.