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...

trimethylamine in the body are associated with the development of trimethylaminuria, or fish odor syndrome, caused by a genetic defect in the enzyme which...

Trimethylaminuria is a rare defect in the production of the enzyme flavin-containing monooxygenase 3 (FMO3). Those suffering from trimethylaminuria are...

objective noninvasive measure of liver failure. A secondary form of trimethylaminuria is also associated with liver failure, and it has been suggested that...

original (PDF) on 2016-03-03. Retrieved 2015-02-23. "Learning About Trimethylaminuria". genome.gov. National Human Genome Research Institute. Kaufmann,...

than FMO3. Genetic deficiencies of the FMO3 enzyme cause primary trimethylaminuria, also known as "fish odor syndrome". FMO3 is also involved in the...

Methylmalonic acidemia Maple syrup urine disease Homocystinuria Tyrosinemia Trimethylaminuria Hartnup disease Biotinidase deficiency Ornithine carbamoyltransferase...

original (PDF) on 2016-03-03. Retrieved 2012-03-03. "Learning About Trimethylaminuria". genome.gov. National Human Genome Research Institute. Kaufmann,...

original (PDF) on 2016-03-03. Retrieved 2017-02-19. "Learning About Trimethylaminuria". genome.gov. National Human Genome Research Institute. Bowen, R....

(TMA) formed by the gut microbes from the unabsorbed choline (see trimethylaminuria). The liver oxidizes TMA to trimethylamine N-oxide (TMAO). Elevated...

dramedy Freaks and Geeks as Gordon Crisp, an optimistic geek with trimethylaminuria. He also appeared in five episodes of Even Stevens and two episodes...

lung infections). Kidney infections and kidney failure. Carcinoma. Trimethylaminuria ("fish odour syndrome"). Diabetes mellitus. Metabolic conditions,...

reporting idiopathic malodor production: demographics and incidence of trimethylaminuria". The American Journal of Medicine. 124 (11): 1058–63. doi:10.1016/j...

clean clothes is also very important especially if you sweat a lot. Trimethylaminuria (TMAU), also known as fish odor syndrome or fish malodor syndrome...

oxidase isolated deficiency Trimethadione antenatal infection Trimethylaminuria Triopia Triosephosphate isomerase deficiency Triphalangeal thumb non...

diseases are already defined and known to cause Bromhidrosis symptoms: Trimethylaminuria Dimethyglycineuria Defects in SELENBP1 gene which leads to accumulation...

L-carnitine) from normal diet, from which seems originate two diseases, trimethylaminuria (or Fish-Odor Syndrome) and cardiovascular disease through the proatherogenic...

L-carnitine) from normal diet, from which seems originate two diseases, trimethylaminuria (or Fish-Odor Syndrome) and cardiovascular disease through the proatherogenic...

geeks. Despite being overweight and having chronic body odour from trimethylaminuria, Gordon tends to be optimistic and take things in stride. Gordon was...

pterygium syndrome prostate cancer Stickler syndrome TAR syndrome trimethylaminuria Usher syndrome Usher syndrome type II Van der Woude syndrome Variegate...

effects of a higher osmotic pressure and peripheral resistance. The trimethylaminuria disorder, also known as fish odor syndrome, causes abnormal FMO3-mediated...

Saccharopinuria 270.8 Other specified disorders of amino-acid metabolism Trimethylaminuria 271 Disorders of carbohydrate transport and metabolism 271.0 Glycogenosis...

reduced TMA N-oxidation capacity resulting in fish odor syndrome Trimethylaminuria. Three forms of the enzyme, FMO1 found in fetal liver, FMO2 found...

reduced TMA N-oxidation capacity resulting in fish odor syndrome Trimethylaminuria. Three forms of the enzyme, FMO1 found in fetal liver, FMO2 found...

revealed a large, undiagnosed population of people suffering from trimethylaminuria, an odor-producing genetic disorder. Preti’s work has frequently been...

reduced TMA N-oxidation capacity resulting in fish odor syndrome Trimethylaminuria. Three forms of the enzyme, FMO1 found in fetal liver, FMO2 found...

Trifunctional protein deficiency; 609015; HADHB Trigonocephaly; 190440; FGFR1 Trimethylaminuria; 602079; FMO3 Triphalangeal thumb, type I; 174500; LMBR1 Triphalangeal...