Neuronopathic Types of Mucopolysaccharidoses: Pathogenesis and Emerging Treatments

• Main Authors: L. A. Osipova (Author), L. M. Kuzenkova (Author), L. S. Namazova-Baranova (Author), A. K. Gevorkyan (Author), T. V. Podkletnova (Author), N. D. Vashakmadze (Author)
• Format: Book
• Published: "Paediatrician" Publishers LLC, 2015-11-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Mucopolysaccharidoses are a group of hereditary metabolic diseases, relating to lysosomal storage disorders and caused by a deficiencyof the enzymes, involved in degradation of glycosaminoglycans (mucopolysaccharides). Severe forms of mucopolysaccharidoses of types I, II and VII and mucopolysacchari...