Literature DB >> 25870212

Fish Malodour syndrome in a child.

Alexandra Oliveira1, Ana Faria1, Mónica Oliva1.   

Abstract

Body odour can be a manifestation of several metabolic diseases. Diagnosis may be difficult because the disease is often unknown to the doctor. We present a child observed in a general paediatric clinic for bad body odour after eating fish. Given the suspicion of trimethylaminuria, molecular study of flavin mono-oxygenase 3 gene was requested. A pathogenic mutation and polymorphism were identified, which could explain the complaint. Dietary and hygienic measures were imposed with symptom improvement. 2015 BMJ Publishing Group Ltd.

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Year:  2015        PMID: 25870212      PMCID: PMC4401951          DOI: 10.1136/bcr-2014-207002

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  12 in total

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

Authors:  Alessandro Pellicciari; Annio Posar; Mauro Andrea Cremonini; Antonia Parmeggiani
Journal:  Brain Dev       Date:  2010-10-20       Impact factor: 1.961

2.  Fish odor syndrome: a case report of trimethylaminuria.

Authors:  Catherine A Ulman; Julian J Trevino; Marvin Miller; Rishi K Gandhi
Journal:  Dermatol Online J       Date:  2014-01-15

3.  Trimethylaminuria associated with seizures and behavioural disturbance: a case report.

Authors:  H W McConnell; S C Mitchell; R L Smith; M Brewster
Journal:  Seizure       Date:  1997-08       Impact factor: 3.184

4.  Trimethylaminuria: the fish malodor syndrome.

Authors:  S C Mitchell; R L Smith
Journal:  Drug Metab Dispos       Date:  2001-04       Impact factor: 3.922

5.  Trimethylaminuria: causes and diagnosis of a socially distressing condition.

Authors:  Richard J Mackay; Christopher J McEntyre; Caroline Henderson; Michael Lever; Peter M George
Journal:  Clin Biochem Rev       Date:  2011-02

6.  Diagnosis and management of trimethylaminuria (FMO3 deficiency) in children.

Authors:  R A Chalmers; M D Bain; H Michelakakis; J Zschocke; R A Iles
Journal:  J Inherit Metab Dis       Date:  2006-02       Impact factor: 4.982

7.  [Primary trimethylaminuria: the fish odor syndrome].

Authors:  Teresa Montoya Alvarez; Patricia Díaz Guardiola; Juana Olivar Roldán; Rosa Elviro; Ron Wevers; Guadalupe Guijarro
Journal:  Endocrinol Nutr       Date:  2009 Jun-Jul

Review 8.  Trimethylaminuria in a girl with Prader-Willi syndrome and del(15)(q11q13).

Authors:  H Chen; F Aiello
Journal:  Am J Med Genet       Date:  1993-02-01

Review 9.  A review of trimethylaminuria: (fish odor syndrome).

Authors:  Jeffrey Messenger; Shane Clark; Susan Massick; Mark Bechtel
Journal:  J Clin Aesthet Dermatol       Date:  2013-11

10.  Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report.

Authors:  Rosalia D'Angelo; Concetta Scimone; Teresa Esposito; Daniele Bruschetta; Carmela Rinaldi; Alessia Ruggeri; Antonina Sidoti
Journal:  J Med Case Rep       Date:  2014-10-06
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  2 in total

1.  Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing.

Authors:  Yiran Guo; Liang-Dar Hwang; Jiankang Li; Jason Eades; Chung Wen Yu; Corrine Mansfield; Alexis Burdick-Will; Xiao Chang; Yulan Chen; Fujiko F Duke; Jianguo Zhang; Steven Fakharzadeh; Paul Fennessey; Brendan J Keating; Hui Jiang; Hakon Hakonarson; Danielle R Reed; George Preti
Journal:  BMC Med Genet       Date:  2017-02-15       Impact factor: 2.103

2.  A case of axillary bromhidrosis secondary to trimethylaminuria successfully treated with microwave-based therapy.

Authors:  Forum Patel; Yingqi Michelle Tu; Stephanie Fernandes; Anne Chapas
Journal:  JAAD Case Rep       Date:  2019-10-07
  2 in total

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