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  2. Mucopolysaccharidosis - Wikipedia

    en.wikipedia.org/wiki/Mucopolysaccharidosis

    Mucopolysaccharidosis is a group of metabolic disorders caused by the absence or malfunctioning of lysosomal enzymes.

  3. Mucopolysaccharidosis type I - Wikipedia

    en.wikipedia.org/wiki/Mucopolysaccharidosis_type_I

    Mucopolysaccharidosis type I is a spectrum of diseases in the mucopolysaccharidosis family. It results in the buildup of glycosaminoglycans (or GAGs, or mucopolysaccharides) due to a deficiency of alpha-L iduronidase , an enzyme responsible for the degradation of GAGs in lysosomes .

  4. Sanfilippo syndrome - Wikipedia

    en.wikipedia.org/wiki/Sanfilippo_syndrome

    Sanfilippo syndrome, also known as mucopolysaccharidosis type III (MPS III), is a rare lifelong genetic disease that mainly affects the brain and spinal cord.It is caused by a problem with how the body breaks down certain large sugar molecules called glycosaminoglycans (also known as GAGs or mucopolysaccharides).

  5. Maroteaux–Lamy syndrome - Wikipedia

    en.wikipedia.org/wiki/Maroteaux–Lamy_syndrome

    Maroteaux–Lamy syndrome, or Mucopolysaccharidosis Type VI (MPS-VI), is an inherited disease caused by a deficiency in the enzyme arylsulfatase B (ARSB). [3] ASRB is responsible for the breakdown of large sugar molecules called glycosaminoglycans (GAGs, also known as mucopolysaccharides).

  6. Sly syndrome - Wikipedia

    en.wikipedia.org/wiki/Sly_syndrome

    Sly syndrome, also called mucopolysaccharidosis type VII (MPS-VII), is an autosomal recessive lysosomal storage disease caused by a deficiency of the enzyme β-glucuronidase. This enzyme is responsible for breaking down large sugar molecules called glycosaminoglycans (AKA GAGs, or mucopolysaccharides).

  7. Vestronidase alfa - Wikipedia

    en.wikipedia.org/wiki/Vestronidase_alfa

    Vestronidase alfa, sold under brand name Mepsevii, is a medication for the treatment of Sly syndrome. [4] It is a recombinant form of the human enzyme beta-glucuronidase.It was approved in the United States in November 2017, to treat children and adults with an inherited metabolic condition called mucopolysaccharidosis type VII (MPS VII), also known as Sly syndrome.

  8. Hurler syndrome - Wikipedia

    en.wikipedia.org/wiki/Hurler_syndrome

    Hurler syndrome, also known as mucopolysaccharidosis Type IH (MPS-IH), Hurler's disease, and formerly gargoylism, is a genetic disorder that results in the buildup of large sugar molecules called glycosaminoglycans (GAGs) in lysosomes.

  9. Morquio syndrome - Wikipedia

    en.wikipedia.org/wiki/Morquio_syndrome

    Morquio syndrome, also known as mucopolysaccharidosis type IV (MPS IV), is a rare metabolic disorder in which the body cannot process certain types of sugar molecules called glycosaminoglycans (AKA GAGs, or mucopolysaccharides).