Glycoproteinosis are lysosomal storage diseases affecting glycoproteins, resulting from defects in lysosomal function. The term is sometimes reserved for conditions involving degradation of glycoproteins.
Types (E77.0) Defects in post-translational modification of lysosomal enzymes Mucolipidosis II (I-cell disease) Mucolipidosis III (pseudo-Hurler polydystrophy) (E77.1) Defects in glycoprotein degradation Aspartylglucosaminuria Fucosidosis Mannosidosis Sialidosis (mucolipidosis I) Another type, recently characterized, is galactosialidosis.
References
External links
NIH Archived 2006-09-05 at the Wayback Machine
