Orphanet: Biochemical diagnosis of fatty acid oxidation defects and organic acidaemias Analyte: Acyl carnitine by tandem MS
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Biochemical diagnosis of fatty acid oxidation defects and organic acidaemias (Analyte: Acyl carnitine by tandem MS)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 14/11/2011
  • Paediatric Metabolic Section, Department of Clinical Biochemistry
  • Newcastle upon Tyne Hospitals NHS Foundation Trust Royal
  • The Great North Children's Hospital, Royal Victoria Infirmary
  • Queen Victoria Road
  • NEWCASTLE UPON TYNE NE1 4LP
  • UNITED KINGDOM
  • Director of laboratory : Dr Kim BARTLETT
  • More information
  • Phone : 44 (0)191 282 4566
  • Additional Phone : -
  • Fax : 44 (0)191 282 4217
  • Website
Last update: November 2011

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay
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List of diseases and genes

List of diseases tested (2)
Classic organic aciduria
Disorder of fatty acid oxidation and ketone body metabolism
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.