Orphanet: Diagnosis of peroxisomal metabolism disorders : very long chain fatty acid analysis GCMS
x

Search for a diagnostic test

* (*) mandatory field

Diagnosis of peroxisomal metabolism disorders : very long chain fatty acid analysis (GC/MS)

  • Centre of Clinical Genetics - United Laboratories
  • Centre of Clinical Genetics - Tartu University Hospital
  • L.Puusepa 2
  • 50406 TARTU
  • ESTONIA
  • Director of laboratory : Dr Tiina KAHRE
  • More information
  • Phone : 37 27 31 94 89
  • Additional Phone : 37 27 31 94 91
  • Fax : 37 27 31 94 84
  • Website
Last update: June 2018

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay
-
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.