Definition of Trimethylaminuria

1. Noun. A rare metabolic disorder that causes a defect in enzyme production and consequent body odour. ¹

¹ Source: wiktionary.com

Medical Definition of Trimethylaminuria

1. An inborn error of metabolism associated with an offensive body odour, the smell of rotting fish, due to the excessive excretion of tma in urine, sweat, and breath. Persons with tma may experience tachycardia (fast heart rate) and severe hypertension (high blood pressure) after eating cheese (which contains tyramine) and after using nasal sprays containing epinephrine. Tma is caused by a mutation (change) in the gene for an enzyme, flavin-containing monooxygenase-3 (fmo3) encoded by a gene on chromosome 1. The fmo3 enzyme metabolises tyramine (which is in cheese). The syndrome is associated with various psychosocial reactions, including social isolation, clinical depression and attempted suicide. (12 Dec 1998)

Lexicographical Neighbors of Trimethylaminuria

trimethoprim
trimethoprim-sulfamethoxazole
trimethoprim-sulfamethoxazole combination
trimethoprim resistance
trimethoprims
trimethoxyamphetamine
trimethoxyamphetamines
trimethyl
trimethylacetate
trimethylacetates
trimethylacetic acid
trimethylaluminum
trimethylamine
trimethylamine-coenzyme M methyltransferase
trimethylamines
trimethylaminuria (current term)
trimethylammonium
trimethylarsine
trimethylate
trimethylated
trimethylates
trimethylating
trimethylation
trimethylations
trimethylbenzene
trimethylbenzenes
trimethylcarbinol
trimethylene
trimethylenebromide
trimethylethylene

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