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Trimethylaminuria.

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke - 28 Sept 2021

Kloster Ida, Erichsen Martina Moter

Abstract excerpt

BACKGROUND: Trimethylaminuria is a rare disorder characterised by foul odour from bodily fluids and breath. The condition is caused by a homozygous mutation in the FMO3 (flavin monooxygenase 3) gene coding for the enzyme that converts TMA (trimethylamine) to trimethylamine N-oxide. The result is elevated levels of secreted trimethylamine, which has a strong odour. The condition is likely to affect mental,...

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PMID: 34597008
DOI: 10.4045/tidsskr.21.0142

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