| 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
References
- ↑ Prayson, Richard A. (2012). Neuropathology. Elsevier Health Sciences. p. 388. ISBN 978-1437709490.
External links
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