1.
Pediatr Dermatol
; 29(3): 369-70, 2012.
Article
in English
| MEDLINE
| ID: mdl-21995841
ABSTRACT
A 10-year-old boy with Hunter syndrome and extensive typical skin lesions underwent 9 months of enzyme replacement therapy, after which the skin lesions disappeared. We believe that treatment with idursulfase probably removes the cutaneous storage of glucosaminoglycans in Hunter syndrome.