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[edit]
See also[edit]
References[edit]
- ^ Prayson, Richard A. (2012). Neuropathology. Elsevier Health Sciences. p. 388. ISBN 978-1437709490.
External links[edit]
| Authority control databases: National |
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