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Mucopolysaccharidosis Type VIII
Also Known As:
Diferrante Syndrome; Glucosamine-6-Sulfate Sulfatase Deficiency; MPS VIII
Networked:
1
relevant articles (
0
outcomes,
0
trials/studies)
Disease Context: Research Results
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Inborn Genetic Diseases: 11939
Inborn Errors Metabolism: 1162
Lysosomal Storage Diseases: 2132
Mucopolysaccharidoses: 1610
Mucopolysaccharidosis Type VIII: 1
Inborn Errors Carbohydrate Metabolism
Mucopolysaccharidoses: 1610
Mucopolysaccharidosis Type VIII: 1
Skin and Connective Tissue Diseases
Connective Tissue Diseases: 3269
Mucinoses: 170
Mucopolysaccharidoses: 1610
Mucopolysaccharidosis Type VIII: 1
Nutritional and Metabolic Diseases: 15
Metabolic Diseases: 10142
Inborn Errors Metabolism: 1162
Lysosomal Storage Diseases: 2132
Mucopolysaccharidoses: 1610
Mucopolysaccharidosis Type VIII: 1
Inborn Errors Carbohydrate Metabolism
Mucopolysaccharidoses: 1610
Mucopolysaccharidosis Type VIII: 1
Experts
1.
Ajanahalli, Raghupathi R
: 1 article (02/2013)
2.
Anegundi, Reshma
: 1 article (02/2013)
3.
Boranaik, Latha
: 1 article (02/2013)
4.
Kashyap, Suma
: 1 article (02/2013)
5.
Krishnagiri, Chaitra
: 1 article (02/2013)
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Mucopolysaccharidosis Type VIII:
1.
Enzymes
IBA
02/01/2013 - "
Depending upon the enzyme which is deficient and the nature of the material that accumulates at various tissues, the MPS is divided into 8 types (MPS I to MPS VIII).
"