Current Approaches to the Treatment of Hunter Syndrome

• Main Authors: Ekaterina Yu. Zakharova (Author), Elena Yu. Voskoboeva (Author), Alla N. Semyachkina (Author), Nato D. Vashakmadze (Author), Amina I. Gamzatova (Author), Svetlana V. Mikhailova (Author), Sergey I. Kutsev (Author)
• Format: Book
• Published: Union of pediatricians of Russia, 2018-10-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is an X-linked hereditary disorder associated with a deficiency of iduronate2-sulfatase (IDS). IDS deficiency provokes the accumulation of dermatan sulfate and heparan sulfate in different tissues. Clinical manifestations of MPS II are heteroge...