Diseases and Disorders, Disorders of Glycoprotein and Glycolipid Degradation
Last Updated: November 9, 2025 Introduction to I-Cell disease I-cell disease (also called mucolipidosis IIA, or mucolipidosis II alpha/beta: ML-IIα/β) is an autosomal recessive disorder that belongs to the family of disorders identified as lysosomal storage disorders....
Diseases and Disorders, Disorders of Glycoprotein and Glycolipid Degradation
Last Updated: November 9, 2025 Introduction to Sialidosis Sialidosis is an autosomal recessive disease that belongs to the family of disorders identified as lysosomal storage disorders. This disorder is characterized by the lysosomal accumulation of...
Diseases and Disorders, Disorders of Glycoprotein and Glycolipid Degradation
Last Updated: November 9, 2025 Introduction to Galactosialidosis Galactosialidosis (also known as Goldberg Syndrome) belongs to the family of disorders identified as lysosomal storage disorders. Galactosialidosis is characterized by the lysosomal accumulation of...
Diseases and Disorders, Disorders of Glycoprotein and Glycolipid Degradation
Last Updated: November 9, 2025 Introduction to Aspartylglucosaminuria Aspartylglucosaminuria is inherited as an autosomal recessive disorder that belongs to the family of disorders identified as lysosomal storage disorders. This disorder is characterized by the...
Diseases and Disorders, Disorders of Glycoprotein and Glycolipid Degradation
Last Updated: November 9, 2025 Introduction to β-Mannosidosis Beta-mannosidosis (β-mannosidosis) is an autosomal recessive disorder that belongs to the family of disorders identified as lysosomal storage disorders. This disorder is characterized by the lysosomal...
