Diseases and Disorders, Disorders of Glycoprotein and Glycolipid Degradation
Last Updated: November 9, 2025 Gangliosides Gangliosides are members of the glycosphingolipid family of glycolipids. Gangliosides are glycosphingolipids that are defined by the presence of N-acetylneuraminic acid (NANA; also known as sialic acid) in varying amounts....
Diseases and Disorders, Disorders of Mucopolysaccharide Metabolism
Last Updated: November 9, 2025 Introduction to Sly Syndrome Sly syndrome is an extremely rare autosomal recessive disease that belongs to the family of disorders identified as lysosomal storage disorders, and historically as the mucopolysaccharidoses. Sly syndrome is...
Diseases and Disorders, Disorders of Mucopolysaccharide Metabolism
Last Updated: November 9, 2025 Introduction to the Hurler and Scheie Syndromes Hurler and Scheie syndromes are autosomal recessive disorders that belong to the family of disorders identified as lysosomal storage disorders, and historically as the mucopolysaccharidoses...
Diseases and Disorders, Disorders of Mucopolysaccharide Metabolism
Last Updated: November 9, 2025 Introduction to Hunter Syndrome Hunter syndrome is an X-linked recessive disorder that belongs to the family of disorders identified as lysosomal storage disorders, and historically as one of the mucopolysaccharidoses, specifically...
