Difference between revisions of "Lysosomal storage diseases"
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'''Lysosomal [[storage diseases]]''' a set of rare | '''Lysosomal [[storage diseases]]''', also '''lysosomal storage disorders''', are a set of rare diseases that are characterized by lysosomal dysfunction. | ||
This grouping includes: | This grouping includes: | ||
*[[Gaucher disease]] - most common. | *[[Gaucher disease]] - most common. | ||
*[[Fabry disease]] - second most common. | *[[Fabry disease]] - second most common. | ||
*[[Cystinosis]]. | |||
*[[Lysosomal acid lipase deficiency]] (Wolman disease). | |||
*Others. | |||
==See also== | ==See also== | ||
Latest revision as of 15:40, 12 June 2017
Lysosomal storage diseases, also lysosomal storage disorders, are a set of rare diseases that are characterized by lysosomal dysfunction.
This grouping includes:
- Gaucher disease - most common.
- Fabry disease - second most common.
- Cystinosis.
- Lysosomal acid lipase deficiency (Wolman disease).
- Others.