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.

Gangliosidosis
SpecialtyEndocrinology Edit this on Wikidata

Types

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See also

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References

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  1. ^ Prayson, Richard A. (2012). Neuropathology. Elsevier Health Sciences. p. 388. ISBN 978-1437709490.
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