Literature DB >> 2713263

An unusual case of trimethylaminuria.

V Ruocco1, M Florio, F G Filioli, V Guerrera, G Prota.   

Abstract

A case is reported of trimethylaminuria that first developed in adulthood without any apparent cause. The patient developed a characteristic fish odour of his sweat, urine and to his breath after the consumption of choline-rich foods. Elevated levels of trimethylamine were present in the urine after dietary tests and identified by means of gas chromatography.

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Year:  1989        PMID: 2713263     DOI: 10.1111/j.1365-2133.1989.tb04175.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  5 in total

1.  Relationships between flavin-containing mono-oxygenase 3 (FMO3) genotype and trimethylaminuria phenotype in a Japanese population.

Authors:  Makiko Shimizu; Charles K Allerston; Elizabeth A Shephard; Hiroshi Yamazaki; Ian R Phillips
Journal:  Br J Clin Pharmacol       Date:  2014-05       Impact factor: 4.335

2.  Trimethylaminuria: causes and diagnosis of a socially distressing condition.

Authors:  Richard J Mackay; Christopher J McEntyre; Caroline Henderson; Michael Lever; Peter M George
Journal:  Clin Biochem Rev       Date:  2011-02

3.  Functional characterization of genetic variants of human FMO3 associated with trimethylaminuria.

Authors:  Catherine K Yeung; Elinor T Adman; Allan E Rettie
Journal:  Arch Biochem Biophys       Date:  2007-05-02       Impact factor: 4.013

4.  Trimethylaminuria.

Authors:  Numaera Sabir; Elizabeth A Jones; Beena Padmakumar
Journal:  BMJ Case Rep       Date:  2016-04-26

Review 5.  A review of trimethylaminuria: (fish odor syndrome).

Authors:  Jeffrey Messenger; Shane Clark; Susan Massick; Mark Bechtel
Journal:  J Clin Aesthet Dermatol       Date:  2013-11
  5 in total

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