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.
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Authors | Alexandra Oliveira, Ana Faria, Mónica Oliva |
Journal | BMJ case reports
(BMJ Case Rep)
Vol. 2015
(Apr 13 2015)
ISSN: 1757-790X [Electronic] England |
PMID | 25870212
(Publication Type: Case Reports, Journal Article)
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Copyright | 2015 BMJ Publishing Group Ltd. |
Chemical References |
- Methylamines
- Oxygenases
- dimethylaniline monooxygenase (N-oxide forming)
- trimethyloxamine
- trimethylamine
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Topics |
- Child, Preschool
- Diagnosis, Differential
- Diet Therapy
(methods)
- Female
- Humans
- Hygiene
- Metabolism, Inborn Errors
(diagnosis, genetics, therapy)
- Methylamines
(metabolism, urine)
- Mutation
- Oxygenases
(genetics, metabolism)
- Polymorphism, Genetic
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