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Postgraduate Medical Journal 1999;75:451-452; doi:10.1136/pgmj.75.886.451
© 1999 BMJ Publishing Group Ltd and The Fellowship of Postgraduate Medicine.
Postgrad Med J 1999;75:451-452 ( August )

Review

Classic diseases revisited

Fish odour syndrome H U Rehman

Department of Medicine, Hull Royal Infirmary, Hull HU3 2JZ, UK

Accepted 20 January 1999

Fish odour syndrome (trimethylaminuria) is a metabolic syndrome caused by abnormal excretion of trimethylamine in the breath, urine, sweat, saliva and vaginal secretions. Trimethylamine is derived from the intestinal bacterial degradation of foods rich in choline and carnitine and is normally oxidised by the liver to odourless trimethylamine N-oxide which is then excreted in the urine. Impaired oxidation of trimethylamine is thought to be the cause of the fish odour syndrome and is responsible for the smell of rotting fish. Certain foods rich in choline exacerbate the condition and the patients have a variety of psychological problems. Recognition of the condition is important as dietary adjustments reduce the excretion of trimethylamine and may reduce the odour. Occasionally, a short course of metronidazole, neomycin and lactulose may suppress production of trimethylamine by reducing the activity of gut microflora.


Keywords: fish odour syndrome; trimethylaminuria


© 1999 by The Fellowship of Postgraduate Medicine

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This article has been cited by other articles:

  • Arseculeratne, G., Wong, A. K. C., Goudie, D. R., Ferguson, J. (2007). Trimethylaminuria (Fish-Odor Syndrome): A Case Report. Arch Dermatol 143: 81-84 [Abstract] [Full Text]  
  • KASHYAP, A S, KASHYAP, S. (2000). Fish odour syndrome. Postgrad. Med. J. 76: 318a-318 [Full Text]  

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