Glycoproteinosis
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]
| Glycoproteinosis | |
|---|---|
| Specialty | Endocrinology  |
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]
gollark: > The 22 nm node may be the first time where the gate length is not necessarily smaller than the technology node designation. For example, a 25 nm gate length would be typical for the 22 nm node.
gollark: As far as I know it *used* to actually be a measure of something, but they hit issues around... 22nm or something, don't really know... and despite said measure not changing very much the processes kept getting better, so they just reduced them.
gollark: I mean, generally if the number goes down the density of the transistors goes up, but it's not an actual measurement of anything.
gollark: They don't correspond to any actual measurement now.
gollark: <@!221827050892296192> They used to actually be represent size of the transistors involved, but they no longer do, so the names are basically just, er, "generations" of process technology.
References
- Charles H. Rodeck; Martin J. Whittle (27 October 2008). Fetal medicine: basic science and clinical practice. Elsevier Health Sciences. pp. 362–. ISBN 978-0-443-10408-4. Retrieved 3 November 2010.
- Robert V. Stick; Spencer J. Williams (2 December 2008). Carbohydrates: the essential molecules of life. Elsevier. pp. 402–. ISBN 978-0-240-52118-3. 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.
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