Current Approaches to the Treatment of Hunter Syndrome
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...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Paediatrician Publishers, LLC
2018-10-01
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Series: | Pediatričeskaâ Farmakologiâ |
Subjects: | |
Online Access: | https://www.pedpharma.ru/jour/article/view/1653 |