Gangliosidosis
Gangliosidosis contains different types of lipid storage disorders[1] caused by the accumulation of lipids known as gangliosides. There are two distinct genetic causes of the disease. Both are autosomal recessive and affect males and females equally.
| Gangliosidosis | |
|---|---|
| Specialty | Endocrinology  |
Types
gollark: Main bus designs are supposed to alleviate that.
gollark: We just pull from the bus and hope everything can sustain the necessary throughput.
gollark: Nobody was to know that I was secretly amazing and brilliant at factorio. That totally* is the case.
gollark: Tomorrow I mean.
gollark: I can engage in relief efforts.
See also
- Sphingolipidoses#Overview for an overview table, including gangliosidosis
References
- Prayson, Richard A. (2012). Neuropathology. Elsevier Health Sciences. p. 388. ISBN 1437709494.
External links
| Classification | |
|---|---|
| External resources |
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.