Gangliosidosis

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 

Types

gollark: Krist is NOT really a cryptocurrency in many important ways.
gollark: No, that is waaaaay harder.
gollark: I guess the KV database thing could be billed for slightly too, and would be publicly readable like the "contract" source.
gollark: This is not* awful.
gollark: Or just offload all storage to krist and query via KristQL, yes.

See also

References

  1. Prayson, Richard A. (2012). Neuropathology. Elsevier Health Sciences. p. 388. ISBN 1437709494.
Classification
External resources


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.