AB106. Study of functional independence of patients with Hunter syndrome (mucopolysaccharidosis type II)

BACKGROUND: Hunter syndrome or mucopolysaccharidosis type II (MPS II) is caused by deficiency of lysosomal enzyme iduronate-2-sulfatase and characterized by neurologic and movement functions. Aims: To evaluate functional independence for patients with Hunter syndrome. METHODS: Study included 17 pati...

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Detalhes bibliográficos
Publicado no:Ann Transl Med
Main Authors: Nguyen, Thu Ha, Do Thi, Mo, Thi, Huong Bui, Thi, Xuan Bui, Thuy, Linh Tran THi, Do Thi, Hoa, Thanh, Hoa Nguyen Thi, Chi, Dung Vu
Formato: Artigo
Idioma:Inglês
Publicado em: AME Publishing Company 2017
Assuntos:
Birth Defects, Dysmorphology, Skeletal Dysplasia, Craniofacial Anomalies
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5641789/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s106
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