Diagnosis and Management of Mucopolysaccharidosis Type II (Hunter Syndrome) in Poland

Diagnosis and Management of Mucopolysaccharidosis Type II (Hunter Syndrome) in Poland

Mucopolysaccharidosis type II (MPS II; also known as Hunter syndrome) is a rare, inherited lysosomal storage disease. The disease is caused by deficiency of the lysosomal enzyme iduronate-2-sulphatase (I2S) due to mutations in the <i>IDS</i> gene, which leads to accumulation of glycosami...

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Bibliographic Details
Main Authors: Zbigniew Żuber, Beata Kieć-Wilk, Łukasz Kałużny, Jolanta Wierzba, Anna Tylki-Szymańska
Format: Article
Language:English
Published: MDPI AG 2023-06-01
Series:Biomedicines
Subjects:
lysosomal storage disease
mucopolysaccharidosis II
Hunter syndrome
enzyme replacement therapy
Online Access:https://www.mdpi.com/2227-9059/11/6/1668

Internet

https://www.mdpi.com/2227-9059/11/6/1668

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