Congenital protein hypoglycosylation diseases

ngenital protein hypoglycosylation diseases Review (10761) Total Article Views Authors: Sparks SE Published Date July 2012 Volume 2012:5 Pages 43 - 54 DOI: http://dx.doi.org/10.2147/TACG.S18673 Received: 08 February 2012 Accepted: 12 April 2012 Published: 05 July 2012 Susan E Sparks Department of Pediatrics, Levine Children's Hospital at Carolinas Medical Center, Charlotte, NC, USA; Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, NC, USA Abstract: Glycosylation is an essential process by which sugars are attached to proteins and lipids. Complete lack of glycosylation is not compatible with life. Because of the widespread function of glycosylation, inherited disorders of glycosylation are multisystemic. Since the identification of the first defect on N-linked glycosylation in the 1980s, there are over 40 different congenital protein hypoglycosylation diseases. This review will include defects of N-linked glycosylation, O-linked glycosylation and disorders of combined N- and O-linked glycosylation.