Sanfilippo syndrome, or Mucopolysaccharidosis III (MPS-III) is a rare autosomal recessive lysosomal storage disease caused by a deficiency in one of the enzymes needed to breakdown the glycosaminoglycan heparan sulfate (which is found in the extra-cellular matrix and on cell surface glycoproteins).
This lysosomal storage disorders is due to deficiency in one of the enzymes needed to breakdown the glycosaminoglycan heparan sulfate (which is found in the extra-cellular matrix and on cell surface glycoproteins). Sanfilippo syndrome, or Mucopolysaccharidosis III (MPS-III) is a rare genetic disease.
Sanfilippo syndrome, or Mucopolysaccharidosis III (MPS-III) is a rare genetic disease. This lysosomal storage disorders is due to deficiency in one of the enzymes needed to breakdown the glycosaminoglycan heparan sulfate (which is found in the extra-cellular matrix and on cell surface glycoproteins).
Sanfilippo syndrome, or Mucopolysaccharidosis III (MPS-III) is a rare genetic disease. This lysosomal storage disorders is due to deficiency in one of the enzymes needed to breakdown the glycosaminoglycan heparan sulfate (which is found in the extra-cellular matrix and on cell surface glycoproteins).