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

See also
  • Sphingolipidoses#Overview for an overview table, including gangliosidosis

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


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