References
Neufeld EF, Muenzer J. The mucopolysaccharidoses. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds.
The Metabolic and Molecular Bases of Inherited Disease
. Vol 3. 8th ed. New York, NY: McGraw-Hill; 2001:3421–3452.
Harmatz P, Giugliani R, Schwartz I, et al. Enzyme replacement therapy for mucopolysaccharidosis VI: a Phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study.
J Pediatr
. 2006;148:533-539.
Swiedler SJ, Beck M, Bajbouj M, et al. Threshold effect of urinary glycosaminoglycans and the walk test as indicators of disease progression in a survey of subjects with Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome).
Am J Med Genet A
. 2005;134:144–150.
Wilcox WR. Lysosomal storage disorders: the need for better pediatric recognition and comprehensive care.
J Pediatr
. 2004;144(5 Suppl):S3–S14.
Miller G, Partridge A. Mucopolysaccharidosis type VI presenting in infancy with endocardial fibroelastosis and heart failure.
Pediatr Cardiol
. 1983;4:61–62.
Smith KS, Hallett KB, Hall RK, Wardrop RW, Firth N. Mucopolysaccharidosis: MPS VI and associated delayed tooth eruption.
Int J Oral Maxillofac Surg
. 1995;24:176–180.
Vougioukas VI, Berlis A, Kopp MV, Korinthenberg R, Spreer J, van Velthoven V. Neurosurgical interventions in children with Maroteaux-Lamy syndrome. Case report and review of the literature.
Pediatr Neurosurg
. 2001;35:35–38.
Meikle PJ, Hopwood JJ, Clague AE, Carey WF. Prevalence of lysosomal storage disorders.
JAMA
. 1999;281:249–254.
Poorthuis BJ, Wevers RA, Kleijer WJ, et al. The frequency of lysosomal storage diseases in The Netherlands.
Hum Genet
. 1999;105:151–156.
Litjens T, Hopwood JJ. Mucopolysaccharidosis type VI: structural and clinical implications of mutations in N-acetylgalactosamine-4 sulfatase.
Hum Mutat
. 2001; 18:282–295.
Gunin AG. Connective tissue [fact sheet]. Department of histology at the medical school of Chuvash State University. Available at:
http://www.histol.chuvashia.com/tab-en/cont-en.htm
. Accessed May 8, 2006.
Muenzer J, Fisher A. Advances in the Treatment of Mucopolysaccharidosis Type I.
N Engl J Med
. 2004;19:1932–1934.
Wraith JE. The mucopolysaccharidoses: a clinical review and guide to management.
Arch Dis Childhood.
1995;72:263–267.
Kakkis ED, Neufeld EF. The mucopolysaccharidoses. In: Berg B, ed.
Principles of Child Neurology
. 1st ed. New York, New York: McGraw-Hill Inc; 1996; 1141–1166.
Harmatz P, Ketteridge D, Giugliani R, et al. Direct comparison of measures of endurance, mobility, and joint function during enzyme-replacement therapy of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): results after 48 weeks in a phase 2 open-label clinical study of recombinant human N-acetylgalactosamine 4-sulfatase.
Pediatrics
. 2005;115:e681–e689.
Caplan S, Bonifacino JS. Lysosomes. In: Gorvel J-P, ed.
Intracellular Pathogens in Membrane Interactions and Vacuole Biogenesis
. New York, NY: Kluwer Academic/Plenum Publishers; 2003:16-30.