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Primary Trimethylaminuria The primary genetic form of the disease comprise the majority of the reported cases, and clinical symptoms confirmed genetically as due to inactivating mutations and less severe polymorphisms in the FMO3 gene reported from populations in the USA (including Caucasians, African Americans, Hispanics and Asians), Canada, UK, Spain, Italy, Korea, Japan, Australia (including a patient of Greek ethnicity), Norway and Thailand

Score of (110) indicates mild problem, (1120) indicates moderate problem, (2130) indicates severe problem, (3140) indicates very severe problem 16

European Journal of Nutrition

Another noteworthy benefit of procaine infusion therapy is its detoxifying effects