Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups

Suzan Wopereis, Éva Morava, Stephanie Grünewald, Maciej Adamowicz, Karin M.L.C. Huijben, Dirk J. Lefeber, Ron A. Wevers

Research output: Contribution to journalArticlepeer-review

28 Scopus citations


Defects in the biosynthesis of N- and core 1 O-glycans may be found by isoelectric focusing (IEF) of plasma transferrin and apolipoprotein C-III (apoC-III). We hypothesized that IEF of transferrin and apoC-III in combination with sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) of apoC-III may provide a classification for congenital disorders of glycosylation (CDG) patients. We analyzed plasma from 22 patients with eight different and well-characterized CDG subtypes and 19 cases with unsolved CDG. Transferrin IEF (TIEF) has been used to distinguish between N-glycan assembly (type 1 profile) and processing (type 2 profile) defects. We differentiated two different CDG type 2 TIEF profiles: The "asialo profile" characterized by elevated levels of asialo- and monosialotransferrin and the "disialo profile" characterized by increased levels of disialo- and trisialotransferrin. ApoC-III IEF gave two abnormal profiles ("apoC-III0" and "apoC-III1" profiles). The results for the eight established CDG forms exactly matched the theoretical expectations, providing a validation for the study approach. The combination of the three electrophoretic techniques was not additionally informative for the CDG-Ix patients as they had normal apoC-III IEF patterns. However, the CDG-IIx patients could be further subdivided into six biochemical subgroups. The robustness of the methodology was supported by the fact that three patients with similar clinical features ended in the same subgroup and that another patient, classified in the "CDG-IIe subgroup," turned out to have a similar defect. Dividing the CDG-IIx patients in six subgroups narrows down drastically the options of the primary defect in each of the subgroups and will be helpful to define new CDG type II defects.

Original languageEnglish (US)
Pages (from-to)1312-1319
Number of pages8
Issue number12
StatePublished - Dec 2005


  • Apolipoprotein C-III SDS-PAGE
  • Apolipoprotein C-III isoelectric focusing
  • Congenital disorders of glycosylation
  • N-glycosylation
  • O-glycosylation
  • Transferrin

ASJC Scopus subject areas

  • General Medicine


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