action myoclonus การใช้

• Mutations in " SCARB2 " have been shown to cause action myoclonus renal failure syndrome, a rare syndrome characterized by progressive neurological disease and associated with proteinuria, kidney failure, and Focal segmental glomerulosclerosis.
• Some studies have shown that doses of 5-hydroxytryptophan ( 5-HTP ) leads to improvement in patients with some types of action myoclonus and PME . These differences in the effect of 5-HTP on patients with myoclonus have not yet been explained.