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Diagnosis and Phenotypic Assessment of Trimethylaminuria, and Its Treatment with Riboflavin: 1H NMR Spectroscopy and Genetic Testing. Orphanet Journal of Rare Diseases, vol

Marks R, Dudley F, Wan A (1978) Trimethylamine metabolism in liver disease

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Clinicians can measure urinary levels of TMA and TMAO either in steady state or after a dietary challenge and can offer genetic testing for known FMO3 variants

When examining feces, the unsporulated oocysts can easily be mistaken for fungal spores, and thus can be easily overlooked