Abstract
Mild to transient trimethylaminuria is caused by common variants in the FMO3 gene leading to greatly reduced enzyme activity in vivo. FMO3 deficiency may have clinical relevance well beyond unpleasant body odour.
MeSH terms
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Adult
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Child
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Genes, Recessive
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Genetic Variation*
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Humans
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Metabolism, Inborn Errors / genetics
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Metabolism, Inborn Errors / urine*
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Methylamines / urine*
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Mutation, Missense
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Oxygenases / deficiency
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Oxygenases / genetics*
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Syndrome
Substances
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Methylamines
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Oxygenases
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dimethylaniline monooxygenase (N-oxide forming)
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trimethylamine