Gangliosidosis

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Gangliosidosis
Classification and external resources
Specialty endocrinology
ICD-10 E75.0-E75.1
ICD-9-CM 330.1
MeSH D005733
Orphanet 309144

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]

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

External links[edit]