Search for a diagnostic test

* (*) mandatory field

Biochemical diagnosis of Congenital Disorders of Glycosylation (Analysis of Transferrin N-glycosylation and ApoCIII O-glycosylation by iso-electric focusing in plasma and CDG-II subtype identification by mass spectrometry of transferrin)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 05/11/2013
  • Translationeel Metabool Laboratorium
  • Afdeling Laboratoriumgeneeskunde
  • Radboudumc - Radboud universitair medisch centrum
  • Geert Grooteplein-Zuid 10
  • 6525 GA NIJMEGEN
  • Director of laboratory : Pr L.P.W.J. [Bert] VAN DEN HEUVEL
  • More information
  • Phone : +31 (0)24 361 4567
  • Additional Phone : -
  • Fax : +31 (0)24 366 8754
  • Website
  • Contact
Last update: November 2013


Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay
Analyte / Enzyme assay

List of diseases and genes

List of diseases tested (1)
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.