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Trimethylaminuria has an autosomal recessive pattern of inheritance. Most cases of trimethylaminuria appear to be inherited in an autosomal recessive pattern, which means two copies of the gene in each cell are altered. The parents of an individual with an autosomal recessive disorder are both carriers of one copy of the altered gene.
Trimethylaminuria is a rare defect in the production of the enzyme flavin-containing monooxygenase 3 (FMO3). [19] [20] Those suffering from trimethylaminuria are unable to convert choline-derived trimethylamine into trimethylamine oxide. Trimethylamine then accumulates and is released in the person's sweat, urine, and breath, giving off a ...
Do you have your personal hygiene covered? ... Trimethylaminuria, a rare metabolic disorder related to enzyme deficiency that causes a fishy odor. Taking certain medications, such as ...
Trimethylaminuria is more common in women, according to the National Human Genome Research Institute. Symptoms can worsen or become more noticeable around puberty, before or during your period ...
Individuals with trimethylaminuria develop a characteristic fish odor—the smell of trimethylamine—in their sweat, urine, and breath after the consumption of choline-rich foods. A condition similar to trimethylaminuria has also been observed in a certain breed of Rhode Island Red chicken that produces eggs with a fishy smell, especially ...
Some people may carry a gene variation that helps them avoid body odor.
2328 14262 Ensembl ENSG00000007933 ENSMUSG00000026691 UniProt P31513 P97501 RefSeq (mRNA) NM_001002294 NM_006894 NM_001319173 NM_001319174 NM_008030 RefSeq (protein) NP_001002294 NP_001306102 NP_001306103 NP_008825 NP_032056 Location (UCSC) Chr 1: 171.09 – 171.12 Mb Chr 1: 162.78 – 162.81 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Flavin-containing monooxygenase 3 (FMO3 ...
Read no further until you really want some clues or you've completely given up and want the answers ASAP. Get ready for all of today's NYT 'Connections’ hints and answers for #619 on Wednesday ...