Gangliosidosis
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
- GM1 gangliosidoses - GM1
- GM2 gangliosidoses - GM2
See also
- Sphingolipidoses#Overview
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 is issued from Offline. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.