Difference between revisions of "Cystinosis"
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==Microscopic== | ==Microscopic== | ||
===Kidney=== | ===Kidney=== | ||
*Giant cell transformation of podocytes.<ref name=pmid21769177/> | *Giant cell transformation of podocytes.<ref name=pmid21769177/><ref name=pmid21030980>{{Cite journal | last1 = Chandra | first1 = M. | last2 = Stokes | first2 = MB. | last3 = Kaskel | first3 = F. | title = Multinucleated podocytes: a diagnostic clue to cystinosis. | journal = Kidney Int | volume = 78 | issue = 10 | pages = 1052 | month = Nov | year = 2010 | doi = 10.1038/ki.2010.341 | PMID = 21030980 }}</ref> | ||
===Urine=== | ===Urine=== | ||
Revision as of 20:42, 10 April 2015
Cystinosis is a lysosomal storage disease and very rare.[1]
General
- Rare.
- Associated with renal failure.
- Autosomal recessive.[1]
Microscopic
Kidney
Urine
- Hexagonal shaped crystals.
Images
See also
References
- ↑ 1.0 1.1 Veys, KR.; Besouw, MT.; Pinxten, AM.; Dyck, MV.; Casteels, I.; Levtchenko, EN. (Jan 2015). "Cystinosis: a new perspective.". Acta Clin Belg: 2295333714Y0000000113. doi:10.1179/2295333714Y.0000000113. PMID 25560059.
- ↑ 2.0 2.1 Sharma, A.; Gupta, R.; Sethi, SK.; Bagga, A.; Dinda, AK. (Apr 2011). "Giant cell transformation of podocytes: A unique histological feature associated with cystinosis.". Indian J Nephrol 21 (2): 123-5. doi:10.4103/0971-4065.78067. PMID 21769177.
- ↑ Chandra, M.; Stokes, MB.; Kaskel, F. (Nov 2010). "Multinucleated podocytes: a diagnostic clue to cystinosis.". Kidney Int 78 (10): 1052. doi:10.1038/ki.2010.341. PMID 21030980.