Gangliosidosis
| Gangliosidosis | |
|---|---|
| Specialty |
Endocrinology  |
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.
Types
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 | |
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| External resources |
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