Fig. 3From: Hurler–Scheie syndrome in Niger: a case seriesTreatment algorithm for patients with a diagnosis of mucopolysaccharidosis type I. DQ developmental quotient, ERT enzyme replacement therapy, HSCT hematopoietic stem cell transplantation, MPS I mucopolysaccharidosis type I, y year. (Fig. 1 from Muenzer et al., 2009 [7])Back to article page