Fish odor syndrome: a case report of trimethylaminuria
Catherine A Ulman1, Julian J Trevino, Marvin Miller
1Wright State University, Boonshoft School of Medicine.
Abstract:
Trimethylaminuria is a rare, autosomal recessive, metabolic disorder that results in accumulation of trimethylamine (TMA), which smells like rotten fish. The chemical is excreted in sweat and urine owing to a deficiency in the enzyme flavin monooxygenase 3 (FMO3). We report a case of trimethylaminuria in a 12-year-old girl. The patient failed treatment with diet and hygiene modification, but achieved symptomatic improvement after a four-month course of metronidazole.
Related Concept Videos
Physical Properties of Amines
Conditioned Taste Aversion
A notable characteristic of conditioned taste aversion is that it often requires only a single...
Urinary Tract Infection III: Diagnostic Studies and Interprofessional Care
Amines to Sulfonamides: The Hinsberg Test
Generally, a primary amine reacts with the Hinsberg reagent to produce an N-substituted benzenesulfonamide. The electron-withdrawing sulfonyl...
Microbiota of the Urogenital Tract
Olfaction
The olfactory receptors are embedded in the cilia of the...


