Glycoproteinosis
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| Glycoproteinosis | |
|---|---|
| Classification and external resources | |
| ICD-10 | E77 |
| ICD-9 | 271, 272.7 |
Glycoproteinosis are lysosomal storage diseases[1] affecting glycoproteins, resulting from defects in lysosomal function. The term is sometimes reserved for conditions involving degradation of glycoproteins.[2]
[edit] 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.[3]
[edit] References
- ^ Charles H. Rodeck; Martin J. Whittle (27 October 2008). Fetal medicine: basic science and clinical practice. Elsevier Health Sciences. pp. 362–. ISBN 9780443104084. http://books.google.com/books?id=xzMeQbHJX0AC&pg=PA362. Retrieved 3 November 2010.
- ^ Robert V. Stick; Spencer J. Williams (2 December 2008). Carbohydrates: the essential molecules of life. Elsevier. pp. 402–. ISBN 9780240521183. http://books.google.com/books?id=alRrZW4D5JoC&pg=PA402. Retrieved 3 November 2010.
- ^ Bonten EJ, Wang D, Toy JN, et al. (June 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. http://www.fasebj.org/cgi/pmidlookup?view=long&pmid=15084520.
[edit] External links
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