- Source: Glycoproteinosis
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