Gangliosidosis
Jump to navigation
Jump to search
| Gangliosidosis | |
|---|---|
 | |
| GM2-gangliosidosis- with a dysmorphic face, protruding forehead, depressed nasal bridge | |
 |
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
References
- ↑ Prayson, Richard A. (2012). Neuropathology. Elsevier Health Sciences. p. 388. ISBN 978-1437709490. Archived from the original on 2022-01-21. Retrieved 2021-10-04.
External links
| Classification | |
|---|---|
| External resources |
 | This article about an endocrine, nutritional, or metabolic disease is a stub. You can help MDWiki by expanding it. |