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Article

Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report.

Journal of medical case reports - 6 Oct 2014

D'Angelo Rosalia, Scimone Concetta, Esposito Teresa, Bruschetta Daniele, Rinaldi Carmela, Ruggeri Alessia, Sidoti Antonina

Abstract excerpt

INTRODUCTION: Trimethylaminuria is a rare inherited disorder due to decreased metabolism of dietary-derived trimethylamine by flavin-containing monooxygenase 3. Several single nucleotide polymorphisms of the flavin-containing monooxygenase 3 gene have been described and result in an enzyme with decreased or abolished functional activity for trimethylamine N-oxygenation thus leading to trimethylaminuria. CASE...

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Source

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Identifiers

PMID: 25288227
DOI: 10.1186/1752-1947-8-328
PMCID: PMC4190592

Genes

FMO3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report.PMID 25288227Read ↗

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