Gangliosidosis contains different types of lipid storage disorders 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

  • GM1 gangliosidoses - GM1
  • GM2 gangliosidoses - GM2

See also

  • Sphingolipidoses#Overview

References

External links



SciELO Brasil GM1 gangliosidosis a case report GM1 gangliosidosis a

GM1 Gangliosidosis Subtypes CureGM1

How is GM1 Gangliosidosis diagnosed?

What is the history of GM1 Gangliosidosis?

Frontiers GM1 Gangliosidosis—A MiniReview