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TMAU can present in two forms: Primary TMAU: A rare genetic disorder caused by mutations in the FMO3 gene, resulting in a congenital deficiency of the enzyme [2]

Mobile technology to increase HIV/HCV testing and overdose prevention/response among people who inject drugs

Freddy Gerngross is a freelance writer for Wirecutter and covers pro-audio gear for B&H Explora

2008 Mole SE, Williams RE, Goebel HH: Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses

Use of iontophoresis with Verapamil and Dexamethasone, applied to the affected areas has been studied[13] but a recent placebo controlled trial failed to show a significant improvement