Gangliosidosis
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| Gangliosidosis | |
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| 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 978-1437709490.
External links[]
| Classification | |
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| External resources |
| show Authority control |
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Categories:
- Autosomal recessive disorders
- Lipid storage disorders
- Rare diseases
- Endocrine, nutritional and metabolic disease stubs