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  2. Mucopolysaccharidosis - Wikipedia

    en.wikipedia.org/wiki/Mucopolysaccharidosis

    4 Treatment. 5 See also. 6 References. ... Mucopolysaccharidosis has an autosomal recessive pattern of inheritance. ... Thickened skin and mild changes in facial ...

  3. Hyaluronidase deficiency - Wikipedia

    en.wikipedia.org/wiki/Hyaluronidase_deficiency

    Hyaluronidase deficiency, also known as Mucopolysaccharidosis type IX or MPS IX, is a condition caused by mutations in the HYAL1 gene, and is characterized by multiple soft-tissue masses. [ 1 ] : 544

  4. 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 .

  5. Hunter syndrome - Wikipedia

    en.wikipedia.org/wiki/Hunter_syndrome

    Hunter syndrome, or mucopolysaccharidosis type II (MPS II), is a rare inherited lysosomal storage disease in which large sugar molecules called glycosaminoglycans (or GAGs or mucopolysaccharides) build up in body tissues.

  6. Could Ozempic Treat This Common Skin Condition? - AOL

    www.aol.com/could-ozempic-treat-common-skin...

    Hidradenitis suppurativa is a chronic inflammatory skin condition that impacts up to two percent of people in the U.S. (That's roughly 6.5 million people.) But while the condition can be ...

  7. 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).

  8. 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).

  9. Scheie syndrome - Wikipedia

    en.wikipedia.org/wiki/Scheie_syndrome

    Scheie syndrome is a disease caused by a deficiency in the enzyme iduronidase, leading to the buildup of glycosaminoglycans (GAGs) in the body. It is the most mild subtype of mucopolysaccharidosis type I; the most severe subtype of this disease is called Hurler Syndrome.