Impact of Enzyme Replacement Therapy on Linear Growth in Korean Patients with Mucopolysaccharidosis Type II (Hunter Syndrome)

Hunter syndrome (or mucopolysaccharidosis type II [MPS II]) arises because of a deficiency in the lysosomal enzyme iduronate-2-sulfatase. Short stature is a prominent and consistent feature in MPS II. Enzyme replacement therapy (ERT) with idursulfase (Elaprase®) or idursulfase beta (Hunterase®) have...

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Bibliografische gegevens
Hoofdauteurs: Cho, Sung Yoon, Huh, Rimm, Chang, Mi Sun, Lee, Jieun, Kwun, Younghee, Maeng, Se Hyun, Kim, Su Jin, Sohn, Young Bae, Park, Sung Won, Kwon, Eun-Kyung, Han, Sun Ju, Jung, Jooyoun, Jin, Dong-Kyu
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: The Korean Academy of Medical Sciences 2014
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Original Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3924006/
https://ncbi.nlm.nih.gov/pubmed/24550654
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2014.29.2.254
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