Trimethylaminuria, mild

MedGen UID:: 864538
•Concept ID:: C4016101
•: Finding

Synonym:	TRIMETHYLAMINURIA, MILD

OMIM®:	136132

Professional guidelines

PubMed

Relationships between flavin-containing mono-oxygenase 3 (FMO3) genotype and trimethylaminuria phenotype in a Japanese population.

Shimizu M, Allerston CK, Shephard EA, Yamazaki H, Phillips IR
Br J Clin Pharmacol 2014 May;77(5):839-51. doi: 10.1111/bcp.12240. PMID: 24028545 Free PMC Article

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Recent clinical studies

Etiology

A spectrum of molecular variation in a cohort of Italian families with trimethylaminuria: identification of three novel mutations of the FM03 gene.

Teresa E, Lonardo F, Fiumara A, Lombardi C, Russo P, Zuppi C, Scarano G, Musumeci S, Gianfrancesco F
Mol Genet Metab 2006 Jun;88(2):192-5. Epub 2006 Apr 4 doi: 10.1016/j.ymgme.2006.02.014. PMID: 16600650

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Diagnosis

Relationships between flavin-containing mono-oxygenase 3 (FMO3) genotype and trimethylaminuria phenotype in a Japanese population.

Shimizu M, Allerston CK, Shephard EA, Yamazaki H, Phillips IR
Br J Clin Pharmacol 2014 May;77(5):839-51. doi: 10.1111/bcp.12240. PMID: 24028545 Free PMC Article

See all (1)

Therapy

Epilepsy and trimethylaminuria: A new case report and literature review.

Pellicciari A, Posar A, Cremonini MA, Parmeggiani A
Brain Dev 2011 Aug;33(7):593-6. Epub 2010 Oct 20 doi: 10.1016/j.braindev.2010.09.007. PMID: 20970269

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Clinical prediction guides

Transient trimethylaminuria related to menstruation.

Shimizu M, Cashman JR, Yamazaki H
BMC Med Genet 2007 Jan 27;8:2. doi: 10.1186/1471-2350-8-2. PMID: 17257434 Free PMC Article

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Trimethylaminuria, mild

Professional guidelines

PubMed

Recent clinical studies

Etiology

Diagnosis

Therapy

Clinical prediction guides

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