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Bone Marrow Transplantation in Children with Hunter Syndrome: Outcome after 7 to 17 Years

✍ Scribed by Nathalie Guffon; Yves Bertrand; Isabelle Forest; Alain Fouilhoux; Roseline Froissart


Book ID
113745064
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
187 KB
Volume
154
Category
Article
ISSN
1097-6833

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Hunter syndrome (mucopolysaccharidosis type 11, or MPS 11) results from a deficiency of iduronate-2-sulfatase (IDS) activity due to a primary genetic defect in the X-chromosomal iduronate-2-sulfatase gene. We have studied a 10-year-old male, diagnosed with Hunter syndrome at age 2 years, who underwe