Fish Malodour syndrome in a child
Alexandra Oliveira1, Ana Faria1, Mónica Oliva1
1Hospital Pediátrico de Coimbra-Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal.
A child with fishy body odour was diagnosed with trimethylaminuria, a metabolic disorder. Genetic testing identified a mutation in the flavin-containing monooxygenase 3 gene, confirming the cause and leading to symptom improvement with dietary changes.
Area of Science:
- Metabolic disorders
- Clinical genetics
- Paediatrics
Background:
- Body odour can indicate underlying metabolic diseases.
- Diagnosis is often challenging due to physician unfamiliarity with rare conditions.
- A distinctive fishy odour suggests specific metabolic pathways may be involved.
More Related Videos
09:28One-step Metabolomics: Carbohydrates, Organic and Amino Acids Quantified in a Single Procedure
Published on: June 25, 2010
04:19Author Spotlight: An Improved Technique for Trimethylamine Detection in Animal-Derived Medicine by Headspace Gas Chromatography-Tandem Quadrupole Mass Spectrometry
Published on: March 10, 2023
Related Concept Videos
Inborn Errors of Metabolism
Urea Cycle
Urinary Tract Calculi III: Medical Management
Overview of Protein Metabolism
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
Physical Properties of Amines
Urine Studies I: Urinalysis
