Mucopolysaccharidoses

Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.

Also Known As:

Mucopolysaccharidosis

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Inborn Errors Metabolism: 1183
    - Lysosomal Storage Diseases: 2180
      - Mucopolysaccharidoses: 1646
    - Inborn Errors Carbohydrate Metabolism
      - Mucopolysaccharidoses: 1646
Skin and Connective Tissue Diseases
- Connective Tissue Diseases: 3325
  - Mucinoses: 170
    - Mucopolysaccharidoses: 1646
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10634
  - Inborn Errors Metabolism: 1183
    - Lysosomal Storage Diseases: 2180
      - Mucopolysaccharidoses: 1646
    - Inborn Errors Carbohydrate Metabolism
      - Mucopolysaccharidoses: 1646

Rita Lucia Marchesiello Selected Research

Rita Lucia Marchesiello Research Topics

Disease

Drug/Important Bio-Agent (IBA)