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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Clinical, biochemical and molecular phenotype of congenital disorders of glycosylation: long-term follow-up

Fig. 1

Isoelectrofocusing (IEF) of serum transferrin isoforms (a pattern for patient with CDG type II, elevated monosialo-, disialo- and trisialotransferrin fraction; b pattern for patient with CDG type I, elevated asialo- and disialotransferrin isoform; c control normal profile; d pattern for patient with mild CDG type I, slightly elevated asialo- and elevated disialotransferrin fraction; e pattern for patient with mixed CDG I/II on galactose supplementation, mild elevated asialo-, monosialo- and disialotransferrin isoforms; f pattern for patient with mixed CDG I/II before treatement, elevated asialo-, monosialo-, and disialotransferrin isoforms)

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