Home > Health > Conditions and Diseases > Nutritional and Metabolic Disorders > Inherited > Trimethylaminuria
Trimethylaminuria (TMAU), also known as fish odor syndrome or fish malodor syndrome, is a rare metabolic disorder that causes a defect in the normal production of the enzyme Flavin containing monooxygenase 3 (FMO3).When FMO3 is not working correctly, the body loses the ability to properly breakdown trimethylamine.
http://abcnews.go.com/Primetime/story?id=2288096
Article describes this disorder and covers FAQs.
http://ghr.nlm.nih.gov/condition=trimethylaminuria
Genetics Home Reference discusses genes related to this disorder, how it is inherited, and other names TMAU is known by.
http://health.groups.yahoo.com/group/Trimethylaminuria/
Yahoo support group. Registration required.
http://dmd.aspetjournals.org/cgi/content/full/29/4/517
Abstract from Drug Metabolism and Disposition. Includes an introduction, history, clinical reports, biochemical features, types, diagnosis, and treatment.
http://www.bbc.co.uk/news/health-26923503
The BBC speaks to a woman with a syndrome which causes her to smell of ‘rotten garbage’ and ‘sewage’ says she wants to educate people about the condition.
Home > Health > Conditions and Diseases > Nutritional and Metabolic Disorders > Inherited > Trimethylaminuria
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