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medullary storage diseases

Tuesday 3 January 2006

Types

- Gaucher diseases (hereditary glcosylceramide lipidosis)

  • type 1 Gaucher disease
  • type 2 Gaucher disease
  • type 3 Gaucher disease

- Niemann-Pick diseases

  • Niemann-Pick disease type A
  • Niemann-Pick disease type B
  • Niemann-Pick disease type C

- Wolman disease
- Fabry disease
- sialidoses
- gangliosidoses

  • GM1 gangliosidosis
  • GM2 gangliosidosis

- fucosidosis
- alpha-mannosidosis
- glycogen storage diseases
- mucopolysaccharidosis
- cystinosis
- primary hyperoxaluria

See also

- sea-blue histiocytosis
- medullary histiocytic lesions (medullary histiocytosis)
- lysososmal storage diseases (lysososmal storage disorders)