Orphanet: Biochemical diagnosis of Peroxisomal Disorders Analyte: Bile Acids, PUFA, Phytanic, Pristanic and Pipecolic Acid, Plasmalogens and Very Long Chain Fatty Acids
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Biochemical diagnosis of Peroxisomal Disorders (Analyte: Bile Acids, PUFA, Phytanic, Pristanic and Pipecolic Acid, Plasmalogens and Very Long-Chain Fatty Acids)

  • Laboratorium Genetische Metabole Ziekten - Metabolietendiagnostiek
  • Afdeling Klinische Chemie
  • Amsterdam UMC, locatie AMC
  • Meibergdreef 9
  • 1105 AZ AMSTERDAM
  • NETHERLANDS
  • Director of laboratory : Pr R.J.A. [Ronald] WANDERS
  • More information
  • Phone : 31 (0)20 566 5393
  • Additional Phone : -
  • Fax : 31 (0)20 696 2596
  • Website
  • Contact
Last update: May 2017

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 (1)
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