Glycoproteinosis: Difference between revisions
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Revision as of 21:32, 6 January 2009
| Glycoproteinosis | |
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| Specialty | Endocrinology  |
Glycoproteinosis (or "glycoprotein storage disorders") are lysosomal storage diseases affecting glycoproteins, resulting from defects in lysosomal function.
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
Another type, recently characterized, is galactosialidosis.[1]
References
- ^ Bonten EJ, Wang D, Toy JN; et al. (2004). "Targeting macrophages with baculovirus-produced lysosomal enzymes: implications for enzyme replacement therapy of the glycoprotein storage disorder galactosialidosis". FASEB J. 18 (9): 971–3. doi:10.1096/fj.03-0941fje. PMID 15084520.
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External links
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